# The Medicines (Veterinary Drugs) (Pharmacy and Merchants' List) Order 1992

S.I. 1992/33 · made 9 January 1992

This Order revokes the Medicines (Veterinary Drugs) (Pharmacy and Merchants' List) (No. 2) Order 1989, as amended.

Made under: Medicines Act 1968 (Section 57, Section 129); European Communities Act 1972 (repealed)

## Introductory text

MEDICINES
Made 9th January 1992
Laid before Parliament 13th January 1992
Coming into force 30th January 1992
The Secretary of State concerned with health in England, the Secretaries of State respectively concerned with health and with agriculture in Scotland and in Wales, the Minister of Agriculture, Fisheries and Food, the Department of Health and Social Services for Northern Ireland and the Department of Agriculture for Northern Ireland, acting jointly, in exercise of the powers conferred by sections 57(1),(2) and (2A) and 129(4) of the Medicines Act 1968 and now vested in them, and of all other powers enabling them in that behalf, after consulting such organisations as appear to them to be representative of interests likely to be substantially affected by the following Order in accordance with section 129(6) of that Act and with the consent of the Treasury in accordance with section 57(2A) of that Act, and the Secretary of State and the Minister of Agriculture, Fisheries and Food, being Ministers designated for the purposes of section 2(2) of the European Communities Act 1972 in relation to medicinal products and the common agricultural policy of the Economic Community, acting jointly, in exercise of the powers conferred on them by the said section 2(2), hereby make the following Order:

## 1 Title and commencement

This Order may be cited as the Medicines (Veterinary Drugs) (Pharmacy and Merchants' List) Order 1992 and shall come into force on 30th January 1992.

## 2 Interpretation and revocation

(1) In this Order, unless the context otherwise requires—
“the Act” means the Medicines Act 1968;
“agricultural requisites” means things used in the cultivation of the soil or in the keeping of animals for the production of food or as game, and equipment used for the collection of produce from animals kept for the production of food and things used for the maintenance of such equipment, and includes any protective clothing but does not include any other kind of human apparel;
“the Department of Agriculture” means the Department of Agriculture for Northern Ireland;
“the Department of Health (N.I.)” means the Department of Health and Social Services for Northern Ireland;
“final medicated feeding stuff” means any substance, not being a medicinal product, which is for use wholly or mainly by being fed to one or more animals for a medicinal purpose, or for purposes that include that purpose, without further processing;
“fish farmer” means—
(a) a person carrying on a business of fish farming or shellfish farming which is registered in a register kept by the Minister or the Secretary of State (as the case may be) pursuant to the Registration of Fish Farming and Shellfish Farming Businesses Order 1985, or
(b) a person to whom a licence has been granted by the Department of Agriculture under section 11 of the Fisheries Act (Northern Ireland) 1966;
“intermediate feed” means a medicated feeding stuff sold, supplied or imported for use wholly or mainly as an ingredient in the preparation of a substance which is to be fed to one or more animals for a medicinal purpose or for purposes that include that purpose, with or without further processing;
“the Minister” means the Minister of Agriculture, Fisheries and Food;
“placing on the market” means the holding for sale or disposal in any other form whatever to third parties, whether or not for consideration, and actual sale or disposal;
“prescription only medicine” means a medicinal product falling within a description or class for the time being specified for the purposes of section 58 of the Act in an Order made under that section;
“qualifying business” means a business involving in whole or in part the retail sale of agricultural requisites;
“the Register of Manufacturers” means the register of persons entitled to incorporate medicinal products in animal feeding stuffs kept respectively by the Department of Agriculture, and the registrar under regulation 3(1) of the Medicines (Medicated Animal Feeding Stuffs) Regulations 1992;
“the Register of Merchants” means the register of merchants in veterinary drugs or intermediate feed kept respectively by the Society and the Department of Health (N.I.), under articles 5(1) and 8(1) of this Order;
“saddlery business” means a business involving in whole or in part the retail sale of saddlery requisites;
“saddlery requisites” means products and equipment used in the keeping of horses or ponies and things used for the maintenance of such equipment, and includes any human apparel used in the keeping of horses or ponies;
“self-service methods” means any method of sale which allows a purchaser to help himself on or before payment;
“sell by retail” includes offer or expose for sale by retail and supply in circumstances corresponding to retail sale, and cognate expressions shall be construed accordingly;
“the Society” means the Royal Pharmaceutical Society of Great Britain;
“a specially authorised person” means, in relation to a veterinary drug—
(a) a person specially authorised, by virtue of a direction of the licensing authority under article 3(1) of the Medicines (Exemptions from Licences) (Special and Transitional Cases) Order 1971, to assemble that drug otherwise than in accordance with a manufacturer’s licence; or
(b) a person specially authorised by the product licence in respect of that drug to sell the drug under the alternative product name specified in the licence;
“veterinary drug” includes a veterinary drug in respect of which a product licence is granted, after the date of coming into force of this Order, containing a provision to the effect that it may be sold by retail only in accordance with a prescription by an appropriate practitioner or by a person referred to in article 3(1), 6(1), 9(1), 11(1) or 13(1) of this Order;
“veterinary drug not on a general sale list” means a veterinary drug which is not of a description or falling within a class, specified in an Order under section 51 of the Act which is for the time being in force ;
“wholesale dealer” means a person for the time being carrying on a business wholly or mainly comprising the sale or supply in bulk of veterinary drugs.
(2) Unless the context otherwise requires, any reference in this Order to a numbered article or Schedule is to the article of, or Schedule to, this Order which bears that number.
(3) The Medicines (Veterinary Drugs) (Pharmacy and Merchants' List) (No.2) Order 1989 , the Medicines (Veterinary Drugs) (Pharmacy and Merchants' List) (No. 2) (Amendment) Order 1990 and the Medicines (Veterinary Drugs) (Pharmacy and Merchants' List) (No. 2) (Amendment No. 2) Order 1990 are hereby revoked.

## 3 Exemptions for merchants in veterinary drugs

(1) The restrictions imposed by section 52 of the Act (restrictions on sale or supply of medicinal products not on a general sale list) shall not apply to the sale by retail of any veterinary drug not on a general sale list by the holder of the product licence in respect of that veterinary drug, by a specially authorised person or by a person entered in the Register of Merchants as a Category 1 merchant, if that veterinary drug is specified in the second column of Schedule 1 and the conditions contained in paragraph (2) below and article 4 are complied with.
(2) No veterinary drug described in paragraph (1) above shall be sold by retail except to a person whom the seller knows, or has reasonable cause to believe, to be a person who has animals under his control for the purposes of, and in the course of carrying on, a business, either as his sole business activity or as a part of his business activities.
(3) The restrictions imposed by section 52 of the Act shall not apply to the sale by retail of any veterinary drug not on a general sale list and not being a prescription only medicine by the holder of the product licence in respect of that veterinary drug, by a specially authorised person or by a person entered in the Register of Merchants as a Category 1 merchant, if—
(a) that veterinary drug—
(i) is a veterinary drug specified in Schedule 2, and
(ii) is intended for incorporation in animal feeding stuffs at a rate below 2 kilograms per tonne of the final medicated feeding stuff, are complied with; or
(b) that veterinary drug—
(i) is a veterinary drug specified in Schedule 2, and
(ii) is intended for incorporation in animal feeding stuffs at a rate of at least 2 kilograms per tonne of the final medicated feeding stuff, are complied with.
(4) No veterinary drug described in paragraph (3) (a) above shall be soldby retail except—
(a) to a person whose name is entered in Part A of the Register of Manufacturers, or
(b) to a fish farmer.
(5) No veterinary drug described in paragraph (3) (b) above shall be sold by retail except—
(a) to a person whose name is entered in Part A or Part B of the Register of Manufacturers, or
(b) to a fish farmer.

## 4 Further conditions for exemption under article 3

(1) No veterinary drug described in article 3(1) or (3) (a) or (b) shall be sold by retail except—
(a) in the container in which it was made up for sale by the manufacturer or, as the case may be, the assembler of the drug,
(b) in a container which has not been opened since the drug was made up for sale in it, and
(c) on premises which are occupied by, and under the control of, the seller at the time of sale and which are capable of being closed so as to exclude the public, on the premises of the seller, condition (c) above shall not apply to the subsequent delivery of that drug to that person.
(2) No veterinary drug described in article 3(1) or (3) (a) or (b) shall be sold by retail by self-service methods.
(3) In respect of any sale by retail of any veterinary drug described in article 3(1) or (3) (a) or (b) the seller shall make a record of the sale containing particulars of—
(a) the date on which the veterinary drug was sold,
(b) the name, quantity and, except where it is apparent from the name, the pharmaceutical form and strength of the veterinary drug sold, and
(c) the name and address of the person to whom the veterinary drug was sold, date of the sale.
(4) No person shall, in the course of a qualifying business carried on by him, sell by retail any veterinary drug described in article 3(1) or (3) (a) or (b) unless his name is entered in the Register of Merchants as a Category 1 merchant in respect of each premises on which the drug is sold or stored.
(5) In paragraph (1) (c) above “premises” includes a stall of a permanent nature situated at a market or an agricultural showground.

## 5 Register of Merchants for the purposes of article 4(4)

(1) For the purposes of article 4(4) the Society and the Department of Health (N.I.) shall each continue to keep a register of persons as being persons entitled, in the course of qualifying businesses carried on by them, to sell by retail on premises in respect of which their names are entered in the register, any veterinary drug described in article 3(1) or (3) (a) or (b) free from the restrictions imposed by section 52 of the Act, if and so long as the conditions contained in articles 3 and 4 are complied with.
(2) Details of premises used for the storage of any veterinary drug described in article 3(1) or (3) (a) or (b) at a different postal address from that of premises used to sell by retail such drug shall be recorded in a register kept under paragraph (1) above.
(3) Where a person who, whilst carrying on a qualifying business elsewhere than in Northern Ireland, makes an application in writing to the Society for his name to be entered in the Society’s Register of Merchants in respect of any premises on which any veterinary drug described in article 3(1) or (3) (a) or (b) is to be sold or stored by him in the course of that qualifying business, the Society shall, subject to paragraphs (8) and (9) below, enter his name in that Register in respect of those premises.
(4) Where a person who, whilst carrying on a qualifying business in Northern Ireland, makes an application in writing to the Department of Health (N.I.) for his name to be entered in the Department of Health’s (N.I.) Register of Merchants in respect of any premises on which any veterinary drug described in article 3(1) or (3) (a) or (b) is to be sold or stored by him in the course of that qualifying business, the Department of Health (N.I.) shall, subject to paragraphs (8) and (9) below, enter his name in that Register in respect of those premises.
(5) Subject to paragraphs (10) and (12) below, a person whose name is entered in the Register of Merchants in respect of any premises shall, in order to retain his name in that Register in respect of those premises in any year subsequent to the year in which his name is first entered in it, in the month of January in any such year make an application in writing to the Society or the Department of Health (N.I.) (as the case may be) for his name to be retained in the Register of Merchants in respect of those premises.
(6) Subject to paragraphs (11) and (12) below, a person whose name is removed from the Register of Merchants in respect of any premises by reason only that he failed either to make proper application for the retention of his name in that Register pursuant to paragraph (5) above or to pay the fee due in respect of the retention of his name in that Register pursuant to paragraph (10) below may, in order to restore his name to that Register in respect of those premises, make an application to the Society or the Department of Health (N.I.) (as the case may be) for his name to be restored to the Register of Merchants in respect of those premises.
(7) There shall be paid to the Society or the Department of Health (N.I.)—
(a) in respect of the entry in the Register of Merchants of the name of any person in respect of any premises on which any veterinary drug described in article 3(1) or (3) (a) or (b) is to be sold or stored a fee of £198 for each such premises;
(b) in respect of the retention in the Register of Merchants of the name of any person in respect of any premises on which any veterinary drug described in article 3(1) or (3) (a) or (b) is to be sold or stored a fee of £124 for each such premises;
(c) in respect of the restoration to the Register of Merchants of the name of any person in respect of any premises on which any veterinary drug described in article 3(1) or (3) (a) or (b) is to be sold or stored a fee of £174 for each such premises.
(8) The Society or the Department of Health (N.I.) shall refuse to enterin its respective Register of Merchants the name of any person in respect of any premises unless that person—
(a) has paid to the Society or the Department of Health (N.I.) (as the case may be) the fee specified in paragraph (7) (a) above for the entry of his name in that Register; and
(b) has given to the Society or the Department of Health (N.I.) (as the case may be) an undertaking in writing that he will comply with the provisions of the Code of Practice for Distributors (Category 1 Agricultural Merchants) Registered for the Sale, Supply and Storage of Licensed Animal Medicines and Medicated Animal Feeding stuffs dated December 1991, and published by the Ministry of Agriculture, Fisheries and Food (being a Code relating to the sale or supply of the veterinary drugs described in article 3(1) or (3) (a) or (b)).
(9) The Society, with the approval of the Minister, or the Department of Health (N.I.), with the approval of the Department of Agriculture, may refuse to enter in its respective Register of Merchants the name of any person in respect of any premises if, in the opinion of the Society or the Department of Health (N.I.) (as the case may be), the premises are unsuitable for the storage or safekeeping of any veterinary drug described in article 3(1) or (3) (a) or (b).
(10) The Society or the Department of Health (N.I.) shall refuse to retain in its respective Register of Merchants in any year subsequent to the year in which his name is first entered in it the name of any person in respect of any premises unless that person has paid to the Society or the Department of Health (N.I.) (as the case may be) on or before 31st January in that year the fee specified in paragraph (7) (b) above for the retention of his name in that Register.
(11) The Society or the Department of Health (N.I.) shall refuse to restore to its respective Register of Merchants the name of any person in respect of any premises unless that person, having made proper application pursuant to paragraph (6) above, has paid to the Society or the Department of Health (N.I.) (as the case may be) the fee specified in paragraph (7) (c) above for the restoration of his name to that Register.
(12) The Society, with the approval of the Minister, or the Department of Health (N.I.), with the approval of the Department of Agriculture, may refuse to retain in or to restore to, or may remove from its respective Register of Merchants the name of any person in respect of any premises if, in the opinion of the Society or the Department of Health (N.I.) (as the case may be)—
(a) that person has failed to observe any of the provisions of the Code of Practice referred to in paragraph (8) (b) above; or
(b) the conditions under which any veterinary drug described in article 3(1) or (3) (a) or (b) is sold by retail on those premises or under which it is stored on those premises (whether immediately prior to retail sale or not) are unsuitable for that purpose.
(13) In respect of any premises the Society or the Department of Health (N.I.) may remove from its respective Register of Merchants the name of any person entered in it, at the request of that person.
(14) The registrar and the Department shall each furnish to the Minister, on or before 1st April in each year, a copy of the Register kept thereby certified to be a true copy of that Register as at a date specified in the certificate, not being later than 1st March in the year in questionand, pending the furnishing of a further copy of the Register in the following year, shall furnish to the Minister at monthly intervals copies of amendments made to the Register in each month following the date so specified.

## 6 Exemptions for merchants in intermediate feed

(1) The restrictions imposed by section 52 of the Act (restrictions on sale or supply of medicinal products not on a general sale list) shall not apply to the placing on the market of any intermediate feed by the holder of a product licence in respect of that intermediate feed, by a specially authorised person or by a person entered in the Register of Merchants as a Category 1 or 2 merchant unless that intermediate feed has been manufactured in accordance with these Regulations pursuant to Council Directive 90/167/EEC (laying down the conditions governing the preparation, placing on the market and use of medicated feeding stuffs in the Community) and then only if that intermediate feed contains a veterinary drug specified in the second column of either Schedule 2 or Schedule 3 and the conditions contained in paragraphs (2) and (6) below and article 7 are complied with.
(2) No intermediate feed described in paragraph (1) above shall be placed on the market or sold by retail except to a person whom the seller knows, or has reasonable cause to believe, to be a person who has animals under his control for the purposes of, and in the course of carrying on, a business, either as his sole business activity or as part of his business activities.
(3) The restrictions imposed by section 52 of the Act shall not apply to the placing on the market of intermediate feed by a person who is entered in the Register of Merchants as a Category 1 or Category 2 merchant, if—
(a) that intermediate feed—
(i) contains a veterinary drug specified in Schedule 2 or 3, and
(ii) is intended for incorporation in animal feeding stuffs at a rate below 2 kilograms per tonne of the final medicated feeding stuff, are complied with; or
(b) that the intermediate feed—
(i) contains a veterinary drug specified in either Schedule 2 or Schedule 3, and
(ii) is intended for incorporation in animal feeding stuffs at a rate of at least 2 kilograms per tonne of the final medicated feeding stuff, are complied with.
(4) No intermediate feed described in paragraph (3) (a) above shall beplaced on the market or sold by retail except—
(a) to a person whose name is entered in Part A of the Register of Manufacturers, or
(b) to a fish farmer.
(5) No intermediate feed described in paragraph (3) (b) above shall be placed on the market or sold by retail except—
(a) to a person whose name is entered in Part A or Part B of the Register of Manufacturers, or
(b) to a fish farmer.
(6) No intermediate feed which contains a prescription only veterinary drug specified in Schedule 3 shall be placed on the market or sold by retail to any person (except as provided for in article 9(6) (a)) except on production by him of a veterinary written direction.

## 7 Further conditions for exemption under article 6

(1) No intermediate feed described in article 6 shall be placed on the market except—
(a) in the container in which it was made up for sale by the manufacturer or, as the case may be, the assembler of the feed,
(b) in a container which has not been opened since the feed was made up for sale in it and,
(c) on premises which are occupied by, and under the control of, the seller at the time of sale and which are capable of being closed so as to exclude the public, feed on the premises of the seller, condition (c) above shall not apply to the subsequent delivery of that feed to that person.
(2) No intermediate feed described in article 6 shall be sold by retail by self-service methods.
(3) In respect of any sale by retail of any intermediate feed described in article 6 the seller shall make a record of the sale containing particulars of—
(a) the date on which the intermediate feed was sold,
(b) the name, identification and quantity of the intermediate feed sold, and
(c) the name and address of the person to whom the intermediate feed was sold, date of the sale.
(4) No person shall, in the course of a qualifying business carried on by him, place on the market or sell by retail any intermediate feed described in article 6 unless his name is entered in the Register of Merchants in respect of each premises on which the intermediate feed is sold or stored or he is already entered as a Category 1 or Category 2 merchant in the Register of Merchants kept pursuant to article 5(1).
(5) In paragraph (1) (c) above “premises” includes a stall of a permanent nature situated at a market or an agricultural showground.

## 8 Register of Merchants for the purposes of article 7(4)

(1) For the purposes of article 7(4) the Society and the Department of Health (N.I.) shall each continue to keep a register of persons as being persons entitled, in the course of a qualifying business carried on bythem, to place on the market or sell by retail on premises in respect of which their names are entered in the register, any intermediate feed described in article 6 free from the restrictions imposed by section 52 of the Act, if and so long as the conditions contained in articles 6 and 7 are complied with.
(2) Details of premises used for the storage of any intermediate feed described in article 6 at a different postal address from that of premises used to place on the market or sell by retail such intermediate feed shall be recorded in a register kept under paragraph (1) above.
(3) Where a person who, whilst carrying on a qualifying business elsewhere than in Northern Ireland, makes an application in writing to the Society for his name to be entered in the Society’s Register of Merchants in respect of any premises on which any intermediate feed described in article 6 is to be sold or stored by him in the course of that qualifying business, the Society shall, subject to paragraphs (8) and (9) below, enter his name in that Register in respect of those premises.
(4) Where a person who, whilst carrying on a qualifying business in Northern Ireland, makes an application in writing to the Department of health (N.I.) for his name to be entered in the Department of Health’s (N.I.) Register of Merchants in respect of any premises on which any intermediate feed described in article 6 is to be sold or stored by him in the course of that qualifying business, the Department of Health (N.I.) shall, subject to paragraphs (8) and (9) below, enter his name in that Register in respect of those premises.
(5) Subject to paragraphs (10) and (12) below, a person whose name is entered in the Register of Merchants in respect of any premises shall, in order to retain his name in that Register in respect of those premises in any year subsequent to the year in which his name is first entered in it, in the month of January in any such year make an application in writing to the Society or the Department of health (N.I.) (as the case may be) for his name to be retained in the Register of Merchants in respect of those premises.
(6) Subject to paragraphs (11) and (12) below, a person whose name is removed from the Register of Merchants in respect of any premises by reason only that he failed either to make proper application for the retention of his name in that Register pursuant to paragraph (5) above or to pay the fee due in respect of retention of his name in that Register pursuant to paragraph (10) below may, in order to restore his name to that Register in respect of those premises, make an application to the Society or the Department of Health (N.I.) (as the case may be) for his name to be restored to the Register of Merchants in respect of those premises.
(7) There shall be paid to the Society or the Department of Health (N.I.)—
(a) in respect of the entry in the Register of Merchants of the name of any person in respect of any premises on which any intermediate feed described in article 6 is to be sold or stored a fee of £115 for each such premises;
(b) in respect of the retention in the Register of Merchants of the name of any person in respect of any premises on which any intermediate feed described in article 6 is to be sold or stored a fee of £72 for each such premises;
(c) in respect of the restoration to the Register of Merchants of the name of any person in respect of any premises on which any intermediate feed described in article 6 is to be sold or stored a fee of £101 for each such premises.
(8) The Society or the Department of Health (N.I.) shall refuse to enter in its respective Register of Merchants the name of any person in respect of any premises unless that person—
(a) has paid to the Society or the Department of Health (N.I.) (as the case may be) the fee specified in paragraph (7) (a) above for the entry of his name in that Register; and
(b) has given the Society or the Department of Health (N.I.) (as the case may be) an undertaking in writing that he will comply with the provisions of the Code of Practice for Distributors (Category 2 Agricultural Merchants) Registered for the Sale, Supply and Storage of Medicated Animal Feeding stuffs dated December 1991, and published by the Ministry of Agriculture, Fisheries and Food (being a Code relating tothe sale or supply of intermediate feed containing the veterinary drugs described in article 6).
(9) The Society, with the approval of the Minister, or the Department of Health (N.I.), with the approval of the Department of Agriculture, may refuse to enter in its respective Register of Merchants the name of any person in respect of any premises if, in the opinion of the Society or the Department of Health (N.I.) (as the case may be), the premises are unsuitable for the storage or safekeeping of any intermediate feed described in article 6.
(10) The Society or the Department of Health (N.I.) shall refuse to retain in its respective Register of Merchants in any year subsequent to the year in which his name is first entered in it the name of any person in respect of any premises unless that person has paid to the Society or the Department of Health (N.I.) (as the case may be) on or before 31st January in that year the fee specified in paragraph (7) (b) above for the retention of his name in that Register.
(11) The Society or the Department of Health (N.I.) shall refuse to restore to its respective Register of Merchants the name of any person in respect of any premises unless that person, having made proper application pursuant to paragraph (6) above, has paid to the Society or the Department of Health (N.I.) (as the case may be) the fee specified in paragraph (7) (c) above for the restoration of his name to that Register.
(12) The Society, with the approval of the Minister, or the Department of Health (N.I.), with the approval of the Department of Agriculture, may refuse to retain in or to restore to, or may remove from its respective Register of Merchants the name of any person in respect of any premises if, in the opinion of the Society or the Department of Health (N.I.) (as the case may be)—
(a) that person has failed to observe any of the provisions of the Code of Practice referred to in paragraph (8) (b) above; or
(b) the conditions under which any intermediate feed described inarticle 6 is sold by retail on those premises or under which it is stored on those premises (whether immediately prior to retail sale or not) are unsuitable for that purpose.
(13) In respect of any premises the Society or the Department of Health (N.I.) may remove from its respective Register of Merchants the name of any person entered in it, at the request of that person.

## 9 Exemptions in respect of (a) veterinary drugs to be incorporated in animal feeding stuffs and (b) intermediate feed

(1) The restrictions imposed by section 52 of the Act shall not apply to the placing on the market of any veterinary drug not on a general sale list nor of any intermediate feed by—
(a) the holder of the product licence in respect the reof;
(b) the holder of a product licence in respect of an intermediate feed containing or consisting of a veterinary drug;
(c) a specially authorised person;
(d) a person whose name is entered in the Register of Merchants as a Category 1 merchant; or, in the case of an intermediate feed, a person whose name is entered in the Register of Merchants as a Category 1 or Category 2 merchant;
(e) a person whose name is entered in Part A of the Register of Manufacturers; or
(f) wholesale dealer,
(i) is or contains a veterinary drug specified in Schedule 2 or, in the case of an intermediate feed, specified in either Schedule 2 or Schedule 3, and
(ii) is intended for incorporation in animal feeding stuffs at a rate below 2 kilograms per tonne of the final medicated feeding stuff, are complied with.
(2) No veterinary drug nor intermediate feed described in paragraph (1) above shall be placed on the market by any of the persons—
(a) specified in paragraph (1) (a) to (d), or, in the case of an intermediate feed, specified in paragraph (1) (e), except to a personwhose name is entered in Part A of the Register of Manufacturers or to a fish farmer;
(b) specified in paragraph (1) (e) or (f), except to a person whose name is entered in Part A of the Register of Manufacturers and who the seller knows, or has reasonable cause to believe, to be a person who does not have animals under his control for the purposes of, or in the course of carrying on, a business, either as his sole business activity or as part of his business activities, except for research or education purposes only.
(3) The restrictions imposed by section 52 of the Act shall not apply to the placing on the market of any veterinary drug not on a general sale list nor of any intermediate feed by—
(a) the holder of the product licence in respect the reof;
(b) the holder of a product licence in respect of an intermediate feed containing or consisting of a veterinary drug;
(c) a specially authorised person;
(d) a person whose name is entered in the Register of Merchants as a Category 1 merchant; or, in the case of an intermediate feed, a person whose name is entered in the Register of Merchants as a Category 1 or Category 2 merchant;
(e) a person whose name is entered in Part A of the Register of Manufacturers; or
(f) wholesale dealer,
(i) is or contains a veterinary drug specified in Schedule 2 or, in the case of an intermediate feed, specified in either Schedule 2 or Schedule 3, and
(ii) is intended for incorporation in animal feeding stuffs at a rate of at least 2 kilograms per tonne of the final medicated feeding stuff, are complied with.
(4) No veterinary drug nor intermediate feed described in paragraph (3) above shall be placed on the market by any of the persons—
(a) specified in paragraph (3) (a) to (d), or, in the case of an intermediate feed, specified in paragraph (3) (e), except to a person whose name is entered in Part A or Part B of the Register of Manufacturers or to a fish farmer;
(b) specified in paragraph (3) (e) or (f), except to a person whose nameis entered in Part A of the Register of Manufacturers and who the seller knows, or has reasonable cause to believe, to be a person who does not have animals under his control for the purposes of, or in the course of carrying on, a business, either as his sole business activity or as part of his business activities, except for research or educational purposes only.
(5) The restrictions imposed by section 52 of the Act shall not apply to the placing on the market of any veterinary drug not on a general sale list nor of any intermediate feed by—
(a) the holder of the product licence in respect thereof,
(b) the holder of a product licence in respect of an intermediate feed containing or consisting of such a veterinary drug,
(c) a specially authorised person,
(d) a person whose name is entered in Part A of the Register of Manufacturers and who does not have animals under his control for the purposes of, or in the course of carrying on, a business, either as his sole business activity or as part of his business activities, except for research or educational purposes, or
(e) a wholesale dealer, veterinary drug specified in Schedule 3 and the conditions contained inparagraph (6) below and article 10 are complied with.
(6) No veterinary drug nor any intermediate feed described in paragraph (5) above shall be placed on the market or sold by retail except—
(a) to a person whose name is entered in Part A of the Register of Manufacturers and whom the seller knows, or has reasonable cause to believe, to be a person who does not have animals under his control for the purposes of, or in the course of carrying on, a business, either as his sole business activity or as part of his business activities, except for research or educational purposes only, or
(b) to a person—
(i) whose name is entered in Part A of the Register of Manufacturers and whom the seller knows, or has reasonable cause to believe, to be a person who has animals under his control for the purposes of, and in the course of carrying on, a business, either as his sole business activity or as part of his business activities but not for research oreducational purposes only, or
(ii) whose name is entered in Part B of the Register of Manufacturers and that veterinary drug or intermediate feed is intended for incorporation in animal feeding stuffs at a rate of at least 2 kilograms per tonne of the final medicated feeding stuff, or
(iii) who is a fish farmer,

## 10 Further conditions for exemption under article 9

(1) No veterinary drug nor intermediate feed such as is described inarticle 9(1), (3) or (5) shall be sold by retail by self-service methods.
(2) In respect of any placing on the market of any veterinary drug described in article 9(1), (3) or (5) the seller shall make a record of the sale containing particulars of—
(a) the date on which the veterinary drug was sold,
(b) the name, quantity and, except where it is apparent from the name, the pharmaceutical form and strength of the veterinary drug sold, and the name, identification and quantity of the intermediate feed sold, and
(c) the name and address of the person to whom the veterinary drug or intermediate feed was sold, date of the sale.
(3) No person, other than a person whose name is entered in Part A of the Register of Manufacturers shall, in the course of a business carried on by him, place on the market or sell by retail any veterinary drug or intermediate feed such as is described in article 9(1), (3) or (5) unless—
(a) before making any such sale he, or a previous owner of the business, has notified the Society, or in the case of a business carried on in Northern Ireland, the Department of Health (N.I.), as appropriate, of the relevant particulars; and
(b) every twelve months after the first notification, whether made by him or by a previous owner, he notifies the Society or the Department of Health (N.I.), as appropriate, of the relevant particulars; and
(c) he notifies the Society or the Department of Health (N.I.), as appropriate, of any change in the relevant particulars which has occurred since the last notification the reof as soon after such change occurs as is reasonably practicable.
(4) In paragraph (3) above “the relevant particulars”, in relation to a business, means the name of the business and the address, or, where appropriate, the location of every premises on which, during the course of the carrying on of that business, veterinary drugs described in article 9(1), (3) or (5) are being, or are during the next twelve months to be, sold or stored.

## 11 Exemptions for merchants in horse wormers

(1) The restrictictions imposed by section 52 of the Act shall not apply to the sale by retail of any veterinary drug not on a general sale list by the holder of the product licence in respect of that veterinary drug, by a specially authorised person or by a person who is for the time being carrying on a qualifying business or a saddlery business if—
(a) that veterinary drug is specified in the second column of Schedule 4, and
(b) the conditions contained in this article are complied with.
(2) No veterinary drug described in paragraph (1) (a) above shall be sold by retail except—
(a) in the container in which it was made up for sale by the manufacturer or, as the case may be, the assembler of the drug,
(b) in a container which has not been opened since the drug was made up for sale in it,
(c) on premises which are occupied by, and under the control of, the seller at the time of sale and which are capable of being closed so as to exclude the public, and
(d) to a person whom the seller knows, or has reasonable cause to believe, to be a person who has in his charge horses or ponies, drug on the premises of the seller, condition (c) above shall not apply to the subsequent delivery of that drug to that person.
(3) No veterinary drug described in paragraph (1) (a) above shall be sold by retail by self-service methods.
(4) In respect of any sale by retail of any veterinary drug described in paragraph (1) (a) above the seller shall make a record of the sale containing particulars of—
(a) the date on which the veterinary drug was sold, and
(b) the name, quantity and, except where it is apparent from the name, the pharmaceutical form and strength of the veterinary drug sold, of the sale.
(5) No person shall, in the course of a qualifying business or a saddlery business carried on by him, sell by retail any veterinary drug described in paragraph (1) (a) above unless his name is entered in the register kept by the Society or the Department of Health (N.I.) under article 12(1) in respect of each premises on which the drug is sold or stored.
(6) In paragraph (2) (c) above “premises” includes a stall of a permanent nature situated at a market or agricultural showground.

## 12 Register for the purposes of article 11(5)

(1) For the purposes of article 11(5), the Society and the Department of Health (N.I.) shall each continue to keep a register of persons as being persons entitled, in the course of qualifying businesses or saddlery businesses carried on by the m, to sell by retail on premises in respect of which their names are entered in the register, any veterinary drug described in article 11(1) (a) free from the restrictions imposed by section 52 of the Act, if and so long as the conditions contained in article 11 are complied with.
(2) Details of premises used for the storage of any veterinary drug described in article 11(1) (a) at a different postal address from that of premises used to sell by retail such drug shall be recorded in a register kept under paragraph (1) above.
(3) Where a person who, whilst carrying on a qualifying business or a saddlery business elsewhere than in Northern Ireland, makes anapplication in writing to the Society for his name to be entered in the register kept by the Society under paragraph (1) above in respect of any premises on which any veterinary drug described in article 11(1) (a) isto be sold or stored by him in the course of that qualifying business or saddlery business, the Society shall, subject to paragraphs (8) and (9) below, enter his name in that register in respect of those premises.
(4) Where a person who, whilst carrying on a qualifying business or a saddlery business in Northern Ireland, makes an application in writing to the Department of Health (N.I.) for his name to be entered in the register kept by the Department of Health (N.I.) under paragraph (1) above in respect of any premises on which any veterinary drug described in article 11(1) (a) is to be sold or stored by him in the course of that qualifying business or saddlery business, the Department of Health (N.I.) shall, subject to paragraphs (8) and (9) below, enter his name in that register in respect of those premises.
(5) Subject to paragraphs (10) and (12) below, a person whose name is entered in the register kept by the Society or the Department of Health (N.I.) under paragraph (1) above in respect of any premises shall, in order to retain his name in the register in respect of those premises in any year subsequent to the year in which his name was first entered in it, in the month of January in any such year make an application in writing to the Society or the Department of Health (N.I.) (as the case may be) for his name to be retained in that register in respect of those premises.
(6) Subject to paragraphs (11) and (12) below, a person whose name is removed from the register kept by the Society or the Department of Health (N.I.) under paragraph (1) above in respect of any premises by reason only that he failed either to make proper application for the retention of his name in the register pursuant to paragraph (5) above or to pay the fee due in respect of the retention of his name in the register pursuant to paragraph (10) below may, in order to restore his name to the register in respect of those premises, make an application in writing to the Society or the Department of Health (N.I.) (as the case may be) for his name to be restored to the register kept by the Society or the Department of Health (N.I.) (as the case may be) under paragraph (1) in respect of those premises.
(7) There shall be paid to the Society or the Department of Health (N.I.)—
(a) in respect of the entry in the register kept by the Society or the Department of Health (N.I.) (as the case may be) under paragraph (1) above of the name of any person in respect of any premises on which any veterinary drug described in article 11(1) (a) is to be sold or stored a fee of £99 for each such premises;
(b) in respect of the retention in the register kept by the Society or the Department of Health (N.I.) (as the case may be) under paragraph (1) above of the name of any person in respect of any premises on which any veterinary drug described in article 11(1) (a) is to be sold or stored a fee of £62 for each such premises;
(c) in respect of the restoration to the register kept by the Society or the Department of Health (N.I.) (as the case may be) under paragraph (1) above of the name of any person in respect of any premises on which any veterinary drug described in article 11(1) (a) is to be sold or stored a fee of £87 for each such premises;whose name is for the time being entered in, or in the course of beingrestored to, the Register of Merchants in respect of those premises asbeing a person entitled to sell or store the reon, during the course of a qualifying business carried on by him, any veterinary drug described in article 3(1) or (3) (a) or (b).
(8) The Society or the Department of Health (N.I.) shall refuse to enterin the register kept by the Society or the Department of Health (N.I.) (as the case may be) under paragraph (1) above the name of any person in respect of any premises unless that person—
(a) has paid to the Society or the Department of Health (N.I.) (as the case may be) the fee specified in paragraph (7) (a) above for the entry of his name in the register; and
(b) has given to the Society or the Department of Health (N.I.) (as the case may be) an undertaking in writing that he will comply with the provisions of the Code of Practice for Saddlers Selling or Supplying Horse Wormers dated December 1991 and published by the Ministry of Agriculture, Fisheries and Food (being a Code relating to the sale or supply of the veterinary drugs described in article 11(1) (a)).
(9) the Society, with the approval of the Minister, or the Department of Health (N.I.), with the approval of the Department of Agriculture, may refuse to enter in the register kept by the Society or the Department of Health (N.I.) (as the case may be) under paragraph (1) above the name of any person in respect of any premises if, in the opinion of the Society or the Department of Health (N.I.) (as the case may be), the premises are unsuitable for the storage or safekeeping of any veterinary drug described in article 11(1) (a).
(10) The Society or the Department of Health (N.I.) shall refuse to retain in the register kept by the Society or the Department of Health (N.I.) (as the case may be) under paragraph (1) above in any year subsequent to the year in which his name is first entered in it the name of any person in respect of any premises unless that person has paid to the Society or the Department of Health (N.I.) (as the case may be) on or before 31st January in that year the fee specified in paragraph (7) (b) above for the retention of his name in the register.
(11) The Society or the Department of Health (N.I.) shall refuse to restore to the register kept by the Society or the Department of Health (N.I.) (as the case may be) under paragraph (1) above the name of any person in respect of any premises unless that person, having made proper application pursuant to paragraph (6) above, has paid to the Society or the Department of Health (N.I.) (as the case may be) the fee specified in paragraph (7) (c) above for the restoration of his name to the register.
(12) The Society, with the approval of the Minister, or the Department of Health (N.I.), with the approval of the Department of Agriculture, may refuse to retain in or to restore to, or may remove from, the register kept by the Society or the Department of Health (N.I.) (as the case may be) under paragraph (1) above the name of any person in respect of any premises if, in the opinion of the Society or the Department of Health (N.I.) (as the case may be)—
(a) that person has failed to observe any of the provisions of the Code of Practice referred to in paragraph (8) (b) above; or
(b) the conditions under which any veterinary drug described in article 11(1) (a) is sold by retail on those premises or under which it is stored on those premises (whether immediately prior to retail sale or not) are unsuitable for that purpose.
(13) In respect of any premises the Society or the Department of Health (N.I.) may remove from the register kept by the Society or the Department of Health (N.I.) (as the case may be) under paragraph (1) above the name of any person entered in it, at the request of that person.

## 13 Exemptions for pharmacists

(1) The restrictions imposed by section 52(c) of the Act shall not apply to the retail sale of a veterinary drug described in article 3(1) or (3) (a) or (b) where the transaction is carried out in a registered pharmacy by a person acting on behalf of a pharmacist.
(2) The restrictions imposed by section 52 of the Act shall not apply to the supply in circumstances corresponding to retail sale of a veterinary drug such as is described in article 9(1), (3) or (5) by a pharmacist, or his agent, to the person to whom the pharmacist has, in accordance with the provisions of the said section 52, sold the drug by retail.

## 14 Exemptions in cases involving another’s default

(1) The restrictions imposed by section 52 of the Act shall not apply to the sale by retail, in compliance with the conditions in articles 3(2),(4) or (5), 4, 6(2), (4) or (5) of a veterinary drug or intermediate feed by a person for the time being carrying on a qualifying business, which drug or intermediate feed that person, having exercised all due diligence, on reasonable grounds believes to be a veterinary drug or intermediate feed described in article 3(1) or (3) (a) or (b) or 6 but which, due to the act or default of another person, is not such a veterinary drug, or intermediate feed.
(2) The restrictions imposed by section 52 of the Act shall not apply to the sale by retail, in compliance with the conditions contained inarticles 9(2) to (6), of a veterinary drug or intermediate feed by a person for the time being carrying on a business described in article 9(1), which drug or intermediate feed that person, having exercised all due diligence, on reasonable grounds believes to be a veterinary drug orintermediate feed described in article 9(1), but which, due to the actor default of another person, is not such a veterinary drug or intermediate feed.
(3) The restrictions imposed by section 52 of the Act shall not apply to the sale by retail, in compliance with the conditions contained in articles 11(2) to (5) and 12, of a veterinary drug by a person for the time being carrying on a qualifying business or a saddlery business, which drug that person, having exercised all due diligence, on reasonable grounds believes to be a veterinary drug described in article 11(1) (a), but which, due to the act or default of another person is not such a veterinary drug.

## 15 Defences

Any person who, in the course of a business carried on by him, places on the market or sells by retail, offers or exposes for sale by retail, or supplies in circumstances corresponding to retail sale, any intermediate feed in accordance with a forged veterinary written direction, shall not be guilty of an offence under this Order if, having exercised all due diligence, he believes on reasonable grounds that the veterinary written direction is genuine.

## Signature

Signed by authority of the Secretary of State for Health
Virginia Bottomley
Minister of State,
Department of Health
6th January 1992
Strathclyde
Parliamentary Under Secretary of State, Scottish Office
8th January 1992
David Hunt
Secretary of State for Wales
8th January 1992
In witness whereof the Official Seal of the Minister of Agriculture, Fisheries and Food is hereunto affixed on 9th January 1992.
L.S.
John Selwyn Gummer
Minister of Agriculture, Fisheries and Food
Sealed with the Official Seal of the Department of Health and Social Services for Northern Ireland this 6th day of January 1992.
L.S.
F. A. Elliott
Permanent Secretary
Sealed with the Official Seal of the Department of Agriculture for Northern Ireland this 7th day of January 1992.
L.S.
W. J. Hodges
Permanent Secretary
We consent.
Sydney Chapman
Thomas Sackville
Two of the Lords Commissioners of Her Majesty’s Treasury
7th January 1992

## Schedule 1 VETERINARY DRUGS

Product Licence No.
Name of Product
1 Growth Promoters
PL 0006/4070
Romensin RDD
2 Coccidiostats
PL 0025/4009
Amprol Plus Solution
3 Anti-Blackhead Preparations
PL 0012/4175
“Emtryl” Soluble
4 Sheep Dips and Ectoparasiticides
PL 0676/4081
Aerosol Poultry Spray
PL 5653/4028
Auriplak
PL 1300/4010
Barricade
PL 1300/4015
Barricade 5 Pour On
PL 0676/4029
Battles Lice and Mange Liquid Dressing
PL 0676/4010
Battles Special BHC Maggot Oil
PL 0676/4042
Battles Supona Based Organophosphorous Summer Fly Dip
PL 0010/4067
Bayticol Scab & Tick Dip Scab Approved
PL 0010/4069
Bayticol Pour-On
PL 0038/4096
Canovel Insecticidal Spray
PL 1300/4011
C Tag 97 Fly Tag/Flectron Fly Tag Attach a Tag
PL 5869/4095
Coopers Border Winter Dip-Scab Approved
PL 0805/4020
Coopers Fly Dip
PL 0038/4119
Coopers Green Label Scab and Tick Dip
PL 5869/4005
Coopers Powerpack Summer Dip
PL 5869/4002
Coopers Powerpack Winter Dip
PL 5869/4104
Coopers Scab Approved Dip (Border Type)
PL 5869/4007
Coopers Spoton Insecticide
PL 5869/4006
Coopers Winter Dip 200
PL 4149/4001
Deodorised Malathion Premium Grade
PL 1476/4018
Deosan Dysect
PL 5654/4020
Deosan Dysect Pour-On
PL 1476/4026
Deosan Flectron Fly Tag
PL 0010/4071
Diazadip All Seasons Scab Approved Sheep Dip
PL 0676/4030
Dog Mange Cure
PL 1978/4001
Ectoral Tablets No. 1, 2 and 3
PL 4055/4031
Farmers Fly and Tick Dip
PL 1447/4109
Flyte 1250
PL 5869/4000140141
1 Grenade Emulsifiable Concentrate 20
2 Stomoxin or Liquid Concentrate
PL 5869/4132
Grenade 2 Pour-On
PL 0676/4019
Improved Sheep Dip
PL 4055/4012
Lice and Mange Remedy
PL 1826/4004
Lice Tick and Mange Dressing (LTM)
PL 2428/4018
Malacide
PL 0676/4012
Malathion 50 Concentrate Poultry Spray
PL 1728/4029
Nuvan Top
PL 1826/4027
Osmonds Northern Fly Dip
PL 1826/4028
Osmonds Scab Approved Gold Fleece Sheep Dip
PL 1826/4001
Osmonds Superfleece Scab Approved Fly Dip
PL 0676/4097
Paracide Plus
PL 1728/4070
Parasol Pour-On
PL 2428/4018
Pharmacide
PL 0038/4068
Porect
PL 0038/4093
Ridect
PL 1447/4106
Ryposect
PL 1300/4012
Shell Tirade Fly Tags
PL 1300/4014
Shell Tirade Spray
PL 0095/4041
Stockguard Insecticide Cattle Ear Tags
PL 5869/4009
Stomoxin Fly Tags
PL 8566/4001
Taktic
PL 1345/4040
Taskill
PL 1728/4006
Topclip Gold Shield Scab Approved Sheep Dip
PL 8566/4003
Topline
PL 1728/4072
Vetrazin Dip
PL 1728/4080
Vetrazin Pour-On
PL 1826/4025
Viper Dip
PL 4055/4000
Viper Winter Dip
PL 1447/4081
Young’s Scab Approved Blotic Sheep Dip
PL 1447/4096
Young’s Cypor
PL 1447/4016
Young’s HCC Pour-On
PL 1447/4118
Young’s Rycoben Sheep (Mineralised)
PL 1447/4119
Young’s Rycoben Cattle (Mineralised)
PL 1447/4103
Young’s Scab Approved Ectomort Summer Dip
PL 1447/4105
Young’s Scab Approved Jason Winter Dip
PL 1447/4080
Young’s Scab Approved Summer Dip
PL 1447/4120
Young’s Seraphos Spray
5 Anthelmintics
PL 0095/4037
Actelmintic Injectable Wormer
PL 1447/4092
Anthelpor
PL 0010/4089
Armadose Breakwormer
PL 5869/4128140141
1 Autoworm Mark III (Pulse Release Cattle Wormer)
2 Repidose Big 5
PL 5869/4129140141
1 Autoworm 6 (Pulse Release Cattle Wormer)
2 Repidose Mid Season
PL 5869/4123140141
1 Autoworm Mark II (Pulse Release Cattle Wormer)
2 Repidose Mark II
PL 0010/4048
Bayverm Armadose
PL 0010/4058
Bayverm pellets 1.9
PL 0010/4064
Bayverm SC 2.5% Suspension Worm Drench
PL 0010/4047
Bayverm Suspension 2.5
PL 0010/4048
Bayverm Suspension 10
PL 8749/4000
Chaneverm
PL 1728/4082
Combinex Cattle
PL 1728/4081
Combinex Sheep
PL 1861/4055
Day’s Worm Drench
PL 2676/4121
Decazole
PL 8751/4011
Dio Horse and Pony Wormer Paste
PL 8669/4000
Downland Fluke and Worm Drench
PL 0010/4074
Drontal Plus
PL 5151/4001
Equidin Paste
PL 3832/4013
Equitac
PL 0025/4027
Equizole Pony Paste
PL 0025/4005
Equizole Powder
PL 0025/4042
Eqvalan Paste for Horses
PL 0242/4018
Flubenol Pellets
PL 0010/4055
Flukombin
PL 3763/4000
Gapex
PL 0201/4006
Hapadex Drench for Cattle
PL 0201/4002
Hapadex Drench for Sheep
PL 0201/4007
Hapadex Soluble Powder for Cattle
PL 0201/4003
Hapadex Soluble Powder for Sheep
PL 0025/4040
Ivomec Injection for Cattle
PL 0025/4043
Ivomec Injection for Pigs
PL 2676/4131
Klomisole
PL 2000/4081
Levacide Low Volume
PL 2000/4049
Levacide Injection
PL 2000/4060
Levacide Worm Drench
PL 8007/4011
Levadin Drench
PL 8007/4010
Levadin Injection
PL 8007/4014
Levadox
PL 8669/4001
Levadren
PL 2000/4080
Levafas Diamond
PL 2000/4068
Levafas Fluke and Worm Drench
PL 3832/4013
Loditac
PL 3832/4066
Loditac 3% Wormer Pellets
PL 0242/4016
Mebenvet (1.2)
PL 0844/4055
Multiwurma
PL 0012/4003
Nemafax Drench
PL 0201/4006
Netobimin
PL 5869/4051
Nilvax
PL 5869/4033
Nilverm Cattle Special/Nemicide Cattle Drench
PL 5869/4086
Nilverm Gold
PL 0029/4040
Nilverm Injection/Bionem
PL 5869/4032
Nilverm Plus Drench
PL 5869/4022
Nilverm Super
PL 0029/4014
Nilzan Drench
PL 5869/4031
“Nilzan” Drench Plus
PL 5869/4030
“Nilzan” Drench Super
PL 5869/4085
Nilzan Gold
PL 2000/4054
Noroverm Worm Drench
PL 0025/4045
Oramec Drench for Cattle
PL 0025/4041
Oramec Drench for Sheep
PL 0242/4008
Ovitelmin
PL 0242/4007
Ovitelmin Bolus
PL 0242/4006
Ovitelmin S & C
PL 0086/4121
Panacur 1.5% Pellets
PL 0086/4105
Panacur 2.5% Suspension
PL 0086/4110
Panacur 4% Powder
PL 0086/4106
Panacur 10% Suspension
PL 0086/4107
Panacur 22 Granules
PL 0086/4119
Panacur Paste
PL 0086/4136
Panacur SC Cattle Wormer
PL 0086/4130
Panacur SC Sheep Wormer
PL 0057/4090
Paratect Flex Bolus
PL 3832/4073
Powacide
PL 0242/4015
Ripercol Pour-On
PL 0242/4005
Ripercol 3.2% Oral
PL 0242/4003
Ripercol 7.5% Injection
PL 0242/4019
Ripercol S 036C
PL 1447/4094
Rycovet Horse and Pony Wormer
PL 5869/4075
Spectril
PL 0057/4060
Strongid-P (Granules)
PL 0057/4076
Strongid Paste for Dogs
PL 0057/4062
Strongid-P Paste
PL 0057/4079
Strongid Suspension for Dogs
PL 0057/4073
Strongid Tablets 35 mg
PL 0057/4074
Strongid Tablets 125 mg
PL 0242/4025
Supaverm
PL 0286/4032
Synanthic
PL 0286/4034
Synanthic DC
PL 0286/4039
Synanthic Horse Paste
PL 0286/4049
Synanthic I/R
PL 0286/4050
Synanthic Multidose 130
PL 0286/4058
Synanthic Multidose Extra
PL 0286/4066
Synanthic Multidose Plus
PL 0286/4047
Synanthic Sel/Co
PL 5869/4061
Systamex Paste 18.5% Horse and Pony Wormer
PL 0003/4127
Systamex Paste 18.5% Horse and Pony Wormer
PL 5869/4092
Systamex Plus Fluke
PL 5869/4156
Systamex Plus Fluke SC
PL 5869/4084140141
1 Systamex Repidose
2 Autoworm with Systamex
PL 5869/4014
Systamex SC
PL 5869/4060140141
1 Systamex 906 Concentrated Cattle Wormer
2 Systamex Handipack
PL 5869/4059
Systamex Worm Drench for Cattle and Sheep
PL 0242/4013
Telmin
PL 0242/4001
Telmin KH
PL 0242/4014
Telmin Paste
PL 4462/4002
Tetramisole Hydrochloride BP (Vet)
PL 0025/4015
Thibenzole Drench
PL 3832/4022
Valbazen 2.5% Total Spectrum Wormer
PL 3832/4023
Valbazen 10% Total Spectrum Wormer
PL 3832/4015
Valbazen 40% Paste
PL 3832/4025
Valbazen C 10% Total Spectrum Wormer
PL 3832/4026
Valbazen SC 2.5% Total Spectrum Wormer
PL 3832/4068
Valbazen SC 10% Total Spectrum Wormer
PL 3832/4016
Valbazen Cattle Wormer Pellets
PL 8476/4002
Verdisol
PL 0012/4172
Vermadax
PL 2676/4120
Vermaject
PL 2676/4155
Vermisole Forte Drench
PL 2676/4120
Vermisole Injection
PL 2676/4121
Vermisole Worm Drench
PL 2676/4131
Vermofas
PL 1728/4080
Vetrazin R Pour-On
PL 3832/4076
Wormguard Injection
PL 0086/4139
Wormex
PL 1447/4091
Young’s Anthelpor 20
PL 1447/4107
Young’s Sure/Rycovet Bental 2.5
PL 1447/4117
Young’s Sure/Rycovet Bental 7.5
PL 1447/4121
Young’s 4% Ricobendazole Drench
PL 1447/4122
Young’s 15
Ricobendazole Drench6 Milk Fever Preparations
PL 5271/4008
Calciflex 20
PL 5271/4009
Calciflex 40
PL 0829/4167
Calcitad 50
PL 0123/4034
Calcibor CBG 20
PL 0123/4035
Calcibor CBG 40
PL 0123/4037
Calcibor CMP 30
PL 0123/4038
Calcibor CMP 40
PL 0123/4039
Calcibor CMP and D
PL 2000/4065
Calciject 20
PL 2000/4069
Calciject New Formula 40
PL 2000/4013
Calciject PMD
PL 1826/4020
Calcium Borogluconate 40
PL 1861/4009
Calcium Borogluconate 40 MP
PL 2676/4041
Calcium Borogluconate 20 PM
PL 2676/4035
Calcium Borogluconate 25 PMD
PL 2676/4042
Calcium Borogluconate 40 PM
PL 2428/4042140141
1 Calcium Borogluconate Injection 20 Pharmacol 20
2 Injection of Calcium Borogluconate 20
PL 2428/4024
Calcium Borogluconate Injection 25 with Phosphorus Magnesium and Dextrose
PL 2324/4076
Calcium Borogluconate Solution CBG 20
PL 2428/4004
Dextrose Injection
PL 2676/4042
Dextrose 40
PL 1596/4010
Duphafral D 3 1000
PL 2324/4078
Injection of Calcium Borogluconate 40 and Magnesium Hypophosphite 2.2 Solution CMP 40
PL 2324/4003
Injection of Calcium Borogluconate 40 w/v CBG-40 No. 2
PL 2324/4002
Injection of Calcium Borogluconate 20 w/v and Magnesium Hypophosphite 3.5 w/v CMP-20 No. 3
PL 2324/4001
Injection of Calcium Borogluconate 20 w/v and Magnesium Hypophosphite 5 w/v and Dextrose 20 w/v CMPD-20 No. 6
PL 2428/4024
Pharmacal 25 PMD
PL 2428/4027
Pharmacal 30 PM
PL 2428/4028
Pharmacal 40
PL 2428/4004
Pharmadex 50
PL 1345/4007
TVL Calcium Borogluconate “Borocal”
7 Warble Fly Treatments
PL 0025/4046
Invomec-F Injection for Cattle
PL 0025/4040
Ivomec Injection for Cattle
PL 0025/4050
Ivomec Pour-On for Cattle
PL 0010/4004
Tiguvon
PL 1447/4077
Young’s Poron 20
Liver Fluke Remedies
PL 1728/4065
Fasinex 5
PL 1728/4067
Fasinex 10
PL 0242/4023
Flukiver
PL 3832/4073
Powacide
PL 0012/4017
Trodax 20
PL 0012/4135
Trodax 34
PL 3832/4022
Valbazen 2.5 Total Spectrum Wormer
PL 3832/4023
Valbazen 10 Total Spectrum Wormer
PL 3832/4025
Valbazen C 10 Total Spectrum Wormer
PL 3832/4026
Valbazen SC 2.5 Total Spectrum Wormer
PL 0029/4020
Zanil Drench
9 Sheep and Cattle Clostridial Vaccines and Antisera
PL 0003/4019
Blackleg Vaccine
PL 0086/4018
Blackleg Vaccine
PL 0086/4016
Braxy Blackleg Black Disease Vaccine
PL 0086/4017
Braxy/Blackleg Vaccine
PL 0003/4021
Covexin
PL 0086/4023
Heptavac
PL 0086/4132
Heptavac P
PL 5869/4101
Lamb Dysentery and Pulpy Kidney Antiserum BP (Vet)
PL 0086/4027
Lambisan
PL 0086/4022
Lambivac
PL 5869/4051
Nilvax
PL 0086/4020
Ovivac
PL 0086/4129
Ovivac P
PL 0086/4091
Perfrivac 8
PL 0086/4092
Perfrivac B
PL 0086/4093
Perfrivac T
PL 0086/4028
Pulpy Kidney Antiserum
PL 0003/4079
Pulpy Kidney Plus Tetanus Vaccine
PL 0086/4029
Pulpy Kidney and Tetanus Vaccine
PL 0003/4067
Quadrivexin
PL 5869/4053
Tasvax 8
PL 1345/4023
Tasvax Gold
PL 0003/4094
Tribovax-T
PL 0003/4069
Trivexin-T
10 Poultry Vaccines
PL 5654/4017
AE
PL 1598/4075
AE Vaccine (Lyophilised)
PL 3359/4024
Avian Encephalomyelitis Vaccine Delvax AE
PL 1598/4001
Avian Encephalomyelitis Vaccine (Living) Calnek Strain
PL 1708/4133
Avian Encephalomyelitis Vaccine (Living) Nobilis
PL 3832/4033
Bronchimune
PL 3832/4041
Combimune
PL 1598/4029
Combined ND (HB 1) and IB (Massachusetts MM) Vaccine (Living)
PL 1598/4028
Combined ND (La Sota) and IB (MM) Vaccine (Living)
PL 3359/4114
Delsuvac AR-Tox
PL 3359/4075
Delvax 1BH Emulsion
PL 3359/4004
Delvax 1B H 52
PL 3359/4003
Delvax 1B H 120
PL 3359/4001
Delvax Marek THV Freeze-dried
PL 3359/4077
Delvax ND Emulsion
PL 3359/4005
Delvax ND HB 1
PL 3359/4035
Delvax ND Hitchner
PL 3359/4006
Delvax ND La Sota
PL 1708/4188
Duck Plague Vaccine Nobilis
PL 5654/4064
Edsilin
PL 1598/4055
Fowl Pox Vaccine (Poxine)
PL 1598/4053
Fowl Pox Vaccine (Poxinet)
PL 1708/4139
Gumboro Disease Vaccine (Living) Nobilis
PL 1598/4077
Ibinac
PL 1598/4076
Ibinac ND
PL 5654/4000
Iblin
PL 5654/4024
Iblin Bivalent
PL 5654/4013
Iblin Live
PL 3832/4056
IB Vaccine (Living) Massachusetts H 52 Strain
PL 3832/4036
IB Vaccine (Living) Massachusetts H 120 Strain
PL 1708/4225
IB Vaccine Nobilis MA 5
PL 1708/4135
Inactivated ND Vaccine (oil emulsion) Newcavac Nobilis
PL 1708/4066
Infectious Bronchitis Vaccine (Living) Nobilis H 52
PL 1708/4065
Infectious Bronchitis Vaccine (Living) Nobilis H 120
PL 1598/4056
Infectious Larygotracheitis Vaccine (LT VAC)
PL 5654/4018
Marek's
PL 3832/4039
Marek’s Disease Vaccine (Living) THV (Strain FC 126) Freeze-dried (Marimune)
PL 1598/4026
Marek’s Disease Vaccine MD-VAC (Living) THV (Witter Strain) Frozen (Wet)
PL 1598/4027
Marek’s Disease Vaccine (Lyophilised) MD-VAC
PL 1708/4149
Marexine HVT Vaccine
PL 1708/4141
Marexine MD
PL 1442/4000
Marexine THV
PL 1942/4000
Marexine THV
PL 1708/4169
Marexine THV/CA
PL 5654/4023
Maridin
PL 5654/4001
Maternalin
PL 5654/4012
Maternalin Plus
PL 5654/4002
Myxilin
PL 5654/4028
Myxilin Bivalent
PL 5654/4029
Myxilin EDS
PL 3318/4000
ND Vaccine (Inactivated) Oil Emulsion
PL 5654/4007
Newcadin
PL 5654/4004
Newcadin Day Old
PL 5654/4006
Newcadin 25
PL 5654/4008
Newcadin L
PL 5654/4020
Newcadin Live B-1
PL 3832/4057
Newcastle Disease Vaccine (Living) Hitchner B 1 Strain
PL 1598/4000
Newcastle Disease Vaccine (Living) La Sota Strain
PL 3832/4053
Newcastle Disease Vaccine (Living) La Sota Strain
PL 1708/4067
Newcastle Disease Vaccine Hitchner B 1 (Living) Nobilis
PL 1708/4142
Newcastle Disease Vaccine Living (Nobilis Clone 30)
PL 1708/4068
Newcastle Disease Vaccine (Living) La Sota
PL 1708/4150
Newcavac & EDS `76 Vaccine
PL 1708/4143
Nobi-Vac Egg Drop Syndrome `76 Vaccine B 14 (Inactivated)
PL 1708/4167
Nobi-Vac Gumboro + EDS `76
PL 1708/4155
Nobi-Vac Gumboro Inactivated
PL 1708/4158
Nobi-Vac Gumboro + ND
PL 1708/4184
Nobi-Vac IB + G + ND
PL 1708/4185
Nobi-Vac IB + ND
PL 1708/4187
Nobi-Vac IB + ND + EDS
PL 1708/4157
Nobi-Vac Triple GNE
PL 1598/4008
Pabac
PL 5654/4022
Paramyxovirus-3 Disease Vaccine
PL 0086/4039
Pasturella Erysipelas Vaccine
PL 1596/4034
Poulvac AE
PL 1596/4040
Poulvac EDS
PL 1596/4029
Poulvac IB Vaccine H 52 (Living)
PL 1596/4030
Poulvac IB Vaccine H 120 (Living)
PL 1596/4027
Poulvac La Sota
PL 1596/4045
Poulvac Marek HVT Vaccine
PL 1596/4025
Poulvac Marek THV
PL 1596/4042
Poulvac ND + EDS
PL 1596/4026
Poulvac ND Vaccine (Living) HB 1
PL 0002/4025
Tremimune
PL 3832/4024
Tremimune
PL 5654/4019
Ultravac
11 Erysipelas Vaccines and Antisera
PL 0086/4164
Colisorb
PL 0086/4152
Erysorb Plus
PL 0086/4054
Erysorb ST
PL 1531/4012
Ferrovac Ery Vaccine
PL 1596/4078
Suvaxyn Erysipelas Vaccine
PL 0086/4007
Swine Erysipelas Antiserum
PL 3317/4110
Swine Erysipelas Vaccine (Inactivated)
PL 0003/4037
Swine Erysipelas Vaccine
12 Salmonella and E. Coli Vaccines and Antisera
PL 0086/4010
Bovisan DPS
PL 0086/4013
Bovivac
PL 0086/4056
Bovivac Plus
PL 0086/4134
Coliovac
PL 3832/4009
Ecopig
PL 0086/4026
Ecosan
PL 5869/4050
Gletvax 5
PL 0086/4049
Grovax
PL 8327/4063
Imocolibov
PL 1708/4157
Nobi-Vac K 99
PL 1708/4186
Nobi-Vac Porcol 5
PL 0086/4012
Porcovac
PL 0086/4113
Porcovac AT
PL 0086/4163
Porcovac Plus
PL 3832/4004
Scourguard I
PL 0086/4048
Serovax
PL 5811/4000
Sow Intagen O/I
PL 1596/4076
Suvaxyn E. Coli P 4
13 Other Sheep and Cattle Vaccines and Antisera
PL 0003/4022
Clovax
PL 5869/4047
Footvax
PL 0003/4004
Louping I 11 Vaccine
PL 5869/4041
Ovine Enzootic Abortion Vaccine (Inactivated)
PL 0086/4133
Ovipast
PL 0086/4094
Pastacidin
PL 3317/4021
Pneumovac
PL 3317/4012
Pneumovac Plus
PL 6078/4007
Websters Vaxall Norot Vaccine
14 Fish Vaccines
PL 4964/4001
Aeromonas Salmonicide Vaccine
PL 4964/4000
Aeromonas Salmonocide Vibrio A
PL 4964/4005
Aquavac Cyprivac CE
PL 4964/4003
Aquavac-Erm
PL 4964/4004
Aquavac Furovac/Immersion
PL 4964/4002
Aquavac-Vibrio
PL 6149/4000
Ermogen
PL 5869/4106
Fiskevac ERM
PL 5869/4102
Fiskevax-V
PL 6149/4002
Furogen B (Immersion) Vaccine
15 Miscellaneous Vaccines and Antisera
PL 0201/4010
AR-PAC P
PL 0003/4017
Carovax
PL 3359/4044
Delsuvac RP
PL 2460/4000
Duck Hepatitis Virus Vaccine Living Attenuated
PL 0086/4021
Haemosan
PL 1708/4195
Nobi-Vac AR-T
PL 1708/4152
Nobi-Vac L.T. K 88
PL 1708/4163
Pigeon Pox Vaccine (Living) Nobilis
16 Local Anaesthetics
PL 3317/4049
Lignavet Plus Injection
PL 2324/4074
Lignocaine Anaesthetic Injection
PL 2000/4029
Lignocaine and Adrenaline Injection
PL 0123/4054
Lignol
PL 2674/4099
Locovetic
PL 0101/4001
MS 222 Sandoz
PL 2428/4021
Pharmacaine
PL 0123/4068
Willcain
7 Others
PL 2324/4043
Acet Ade
PL 3893/4092
Ash-fer 100
PL 6988/4000
Bloat Guard Premix
PL 6988/4000
Bloat Guard Drench
PL 3832/4065
Bloat Guard Liquid
PL 1861/4048
Cocom
PL 8751/4007
Codifer 8
PL 0010/4009
Coforta 10
PL 5869/4159
Coopercare 1
PL 0012/4184
Copacaps
PL 3317/4010
Copper Methionine Injection
PL 1345/4066
Copagro
PL 0038/4088
Copporal 2 g
PL 0038/4089
Copporal 4 g
PL 0038/4090
Copporal 24 g
PL 0038/4078
Copprite 2 g
PL 0038/4084
Copprite 4 g
PL 0038/4087
Copprite 24 g
PL 1861/4040
Covas
PL 5869/4070
Cujec
PL 0832/4002
Curacho Embrocation
PL 0123/4088
Dalophylline Gel
PL 0086/4035
Defungit
PL 2324/4006
Injection of Dextrose 50 D-50 No. 8
PL 2676/4127
Dextrose 20
PL 0100/4047
Dicarocide Fortie Injection
PL 3656/4012
Dio-Iron
PL 1596/4019
Duphafral Ade Forte
PL 4543/4000
Ferrodown 10
PL 3317/4044
Ferrofax 10 Plus
PL 4543/4001
Ferrodown 20
PL 0208/4003
Ferrowade
PL 0113/4005
Fisons Multivitamins Injection
PL 0113/4006
Fisons Vitamin A, D & E Injection
PL 5764/4000
Footrite
PL 1937/4015
Formaldehyde Solution
PL 0113/4007
Gleptosil
PL 1937/4011
Granulated Copper Sulphate
PL 0113/4012
Hemofer
PL 0113/4000
Imposil
PL 1826/4015
Improved Medicine for Slow Fever
PL 2000/4017
Intravit 12
PL 0829/4117
Iron Dextran 10 (Pharmacosmos)
PL 2676/4049
IRT Concentrated
PL 0829/4011
Kopertox Aerosol
PL 0043/4000
Leodex 10
PL 0043/4036
Leodex 10 Plus
PL 0043/4042
Leodex 20
PL 5271/4006
Magnaflex
PL 5271/4002
Magniflex
PL 2324/4008
Injection of Magnesium Sulphate 25 w/v MS-25 No. 9
PL 2676/4047
Magnesium Sulphate
PL 0123/4054
Magnesium Sulphate Injection
PL 2000/4043
Magnesium Sulphate Injection 25 w/v
PL 2592/4059
Microdex
PL 1861/4020
Morion
PL 3317/4020
Multivet Injection
PL 2676/4013
Multivitamin Injection
PL 2000/4023
Multivitamin Injection
PL 1861/4052
Nedasol
PL 0010/4070
Negasunt
PL 3832/4082
Nordalyte HE
PL 1861/4019
Nuphasol E
PL 1861/4053
Nuphasol 4:1
PL 0676/4090
Orfoids-Capsules for Orf
PL 3405/4043
Peter Hand Iron Dextran 20
PL 2428/4017
Pharmamag 25
PL 2428/4007
Pharmavit AD 3E
PL 6128/4010
Pharmsure Iron Dextran 20
PL 3832/4044
Pragmatar Shampoo
PL 8476/4001
Ridect Fly Tags/Debantic Ear Tags
PL 1011/4001
Roscofer 10 Vet
PL 1011/4000
Roscoral Vet
PL 3821/4000
Rumbul Rumen Bullet Cattle
PL 3821/4001
Rumbul Rumen Bullet Sheep
PL 4031/4002
Rycovet Cuvine
PL 1861/4005
Scour Mixture
PL 3317/4077
Sildex
PL 1598/4007
Spray Diluent
PL 2676/4009
Supercal 20
PL 2676/4041
Supercal 20 PM
PL 2676/4035
Supercal 25 PMD
PL 2676/4040
Supercal 30 PM
PL 2676/4010
Supercal 40
PL 2676/4042
Supercal 40 PM
PL 2100/4035
Surefoot
PL 1598/4065
Suvaxyn Iron Dextran 20 Injection
PL 3862/4000
Synthite Foursure Liquid
PL 0829/4117
Tendex
PL 3317/4128
Tensolvet
PL 0676/4062
Terebene Sheep Balsam
PL 2676/4011
Triave
PL 1393/4023
Veterinary Iron Injection
PL 3317/4047
Vetrivite Plus
PL 0829/4121
Vital Multivitamin Solution
PL 3317/4015
Multivet Vitamin B 12 Injection 1000 054g/ml
PL 0829/4032
Vitamin B 12 Injection
PL 2592/4010
Vitasol
PL 0208/4002
Wade Iron 10
PL 0208/4001
Wade Iron 20
PL 0012/4122
Water for Injections
PL 1861/4010
Wound Powder
PL 1447/4037
Young’s Bovicoppa Items shown in italics did not appear in the Schedule to S.I. 1990/2496.
Alternative product names used by specially authorised persons are not shown.

## Schedule 2 VETERINARY DRUGS (OTHER THAN PRESCRIPTION ONLYMEDICINES) FOR INCORPORATION IN ANIMAL FEEDING STUFFS

Product Licence No.
Name of Product
1 Growth Promoters
PL 2805/4005
Albac Feed Supplement 22
PL 2805/4003
Albac Feed Supplement 55
PL 2805/4002
Albac Feed Supplement 100
PL 2805/4000
Albac Feed Supplement 150
PL 2805/4001
Albac Lactodispersable 100
PL 3405/4030
Avoparcin-20
PL 3405/4019
Avoparcin 50 Premix
PL 0095/4026
Avotan 50
PL 0095/4028
Avotan 50c Avoparcin
PL 0095/4036
Avotan Super
PL 0095/4053
Avotan Super G
PL 0095/4039
Avotan Farm Mix
PL 3405/4026
Bambermycin-5
PL 3405/4047
Bambermycin-20
PL 3405/4046
Bambermycin-40
PL 0010/4043
Bayo-n-ox 10% Premix
PL 3832/4020
Eskalin 20
PL 3832/4031
Eskalin 100
PL 3832/4017
Eskalin 500
PL 3832/4021
Eskalin S-400
PL 5869/4099
Fedan 10% Premix
PL 0086/4031
Flavomycin 5
PL 0086/4148
Flavomycin 80
PL 10101/4003
FPL 50 “ABCHEM”
PL 5811/4001
Intagen Premix
PL 0006/4077
Maxus 25 Premix Poultry
PL 0006/4068
Maxus G 100
PL 10101/4004
Monensin 100 “ABCHEM”
PL 3405/4031
Monensin-20 Ruminant
PL 3405/4022
Monensin-100 Ruminant
PL 0006/4052
Romensin G 100
PL 2411/4000
Rumenox-20
PL 2411/4001
Rumenox-100
PL 0086/4141
Salocin 120
PL 6051/4000
Spira 200
PL 6051/4001
Spira 200L
PL 0006/4051
Tylamix 20 g/kg
PL 0006/4055
Tylamix G 100
PL 0006/4062
Tylamix G 250
PL 3405/4028
Tylosin-20
PL 3405/4007
Tylosin 100 Premix
PL 10101/4002
Tylosin 250 “ABCHEM” Premix
PL 3405/4027
Virginiamycin 20
PL 10101/4001
Virginiamycin 250 “ABCHEM”
PL 3405/4015
ZB-100
PL 3405/4005
ZB 150
PL 0109/4001
Zinc Bacitracin Premix
2 Coccidiostats
PL 0025/4008
Amprolmix
PL 0031/4011
Avatec Premix
PL 0006/4075
Carbigran Premix
PL 3405/4017
Clopidol
PL 3405/4025
Clopidol 250
PL 0621/4001
Coyden 25
PL 0095/4000
Cycostat 66
PL 0095/4042
Cygro Premix
PL 8327/4038
Deccox Pure
PL 0012/4052
Deccox Premix Decoquinate 6
PL 8327/4066
Deccox Sheep Premix
PL 10101/4000
Dinitolmide
PL 0109/4000
Dinormix SR 25
PL 0109/4002
DOT (Dinitolmide)
PL 0006/4047
Elancoban G 200
PL 3405/4006
Monensin 200
PL 3405/4034
Halofuginone-3
PL 8327/4049
Lerbek
PL 0006/4078
Maxiban G 160
PL 3405/4032
Monensin-50 Poultry
PL 3405-4031
Monensin-20 Ruminant
PL 3405/4021
Monensin-100 Poultry
PL 3405/4022
Monensin-100 Ruminant
PL 3405/4006
Monensin-200
PL 10101/4004
Monensin 100 “ABCHEM” Premix
PL 0006/4061
Monteban G 100
PL 3405/4050
Nicarbazin-50
PL 3405/4044
Nicarbazin-250
PL 0025/4019
Nicrazin (Premix)
PL 0086/4135
Sacox 120
PL 1598/4036
Salcostat
PL 1598/4033
Salcostat (DOT) Premix 25
PL 3405/4033
Salgain-30
PL 3405/4053
Salgain-60
PL 0086/4117
Stenorol
PL 0086/4153
Stenorol for Pheasants
PL 4188/4004
Unicox Pure
3 Anti-Blackhead Preparations
PL 3405/4009
Dazole Premix
PL 8327/4034
“Emtryl” Premix
PL 8327/4030
“Emtryl” Pure
PL 3636/4001
Lutrizol — PML Turkeys
PL 2592/4081
Microvet Premix
4 Anthelmintics
PL 0086/4144
Fenbendazole
PL 0242/4018
Flubenol Pellets
PL 0242/4017
Flubenol Premix
PL 3832/4070
Loditac 20
PL 3832/4069
Loditac 200
PL 3832/4066
Loditac 3% Wormer Pellets
PL 3636/4001
Lutrizole
PL 0242/4016
Mebenvet (1.2%)
PL 0242/4020
Mebenvet (5%)
PL 8327/4020
Nemafax 14
PL 0086/4110
Penacur 4% Powder
PL 8476/4000
Verdipor
PL 8476/4002
Verdisol
5 Others
PL 6988/4000
Bloat Guard Premix
PL 2987/4003
Copper (Cupric) Carbonate
PL 2987/4000
Copper Sulphate
PL 2987/4002
Cupric Oxide Items shown in italics did not appear in the Schedule to S.I. 1990/2496.
Alternative product names used by specially authorised persons are not shown.

## Schedule 3 PRESCRIPTION ONLY MEDICINES FOR INCORPORATION IN ANIMAL FEEDINGSTUFFS

Product Licence No.
Name of Product
PL 8007/4019
Amoxinsol 50
PL 3832/4078
Antibac 100
PL 0006/4053
Apralan Soluble Powder
PL 0012/4189
Apralan Soluble Powder
PL 0006/4057
Apralan 20 Premix
PL 0006/4058
Apralan 100 Premix
PL 0012/4191
Apralan 100 Premix
PL 3405/4059
Aquacil
PL 3405/4056
Aquinox
PL 0095/4046
Aureomycin Soluble Powder
PL 2592/4088
Aureosup 100
PL 0095/4048
Aurofac 100 Feed Additive
PL 0095/4047
Aurofac 200 MA Milk Replacer Additive
PL 4188/4018
Auromix 100
PL 1728/4076
Cosumix Plus
PL 3405/4024
CTC-100
PL 0095/4052
Cyfac HS Feed Additive
PL 3405/4010
Dazole Prescription Premix
PL 1596/4113
Duphatrim Poultry Formula
PL 0201/4019
Euphyllin
PL 0012/4159
“Emtryl” Prescription Premix
PL 0012/4160
“Emtryl” Prescription Pure
PL 0012/4161
“Emtryl” Prescription Soluble
PL 1596/4018
Engemycin 5 Soluble Powder
PL 3317/4023
Framomycin Feed Additive
PL 5869/4125
Fulcin Feed Additive
PL 3405/4023
Furazolidone-200
PL 3405/4012
Furazolidone BP
PL 0131/4002
Furazolidone BPC 68
PL 6687/4000
Furazolidone BV
PL 3058/4000
Furazolidone NF BVC
PL 2592/4036
Furazolidone Premix
PL 8007/4022
Grisol-V-Granules
PL 5654/4071
Grisovin Powder
PL 0032/4084
Lincocin Premix
PL 3636/4002
Lutrizol — POM Swine and Turkeys
PL 2592/4083
Micro-Bio Sulphadimidine Premix
PL 2592/4084
Micro-Bio Sulphadimidine Pure
PL 2592/4085
Microfac H P
PL 8007/4026
Navilox
PL 0032/4111
Neobiotic Soluble Powder 70
PL 1598/4037
Nifulidone Premix 11.6
PL 1598/4037
Nifulidone Premix 22.4
PL 1598/4037
Nifulidone Premix 44.8
PL 2000/4084
Norofulvin Granules
PL 6128/4002
Pharmsure Dimetridazole 20
PL 3405/4054
Potencil
PL 3405/4058
Sulfatrim
PL 3405/4055
Synutrim 300
PL 3405/4061
Synutrim 30 Soluble
PL 0057/4089
Terramycin Feed Supplement 20
PL 0057/4080
Terramycin Feed Supplement 10
PL 0057/4083
Terramycin Soluble Powder Concentrate 20
PL 0057/4084
Terramycin Soluble Powder
PL 8007/4018
Tetcin Premix
PL 4188/4020
Tetramin 100
PL 4188/4023
Tetramin 200
PL 3405/4057
Tetraplex
PL 0043/4045
Tiamutin 2 Premix
PL 0043/4057
Tiamutin 25 Premix
PL 5869/4119
Tribrissen SQX Poultry Formula
PL 8007/4023
Trimediazine 15 Premix
PL 8007/4024
Trimediazine 30 Premix
PL 0006/4056
Tylan Premix
PL 0006/4045
Tylan Premix 20 g/kg
PL 0006/4056
Tylan Premix 100 g/kg
PL 0006/4088
Tylasul Premix 50
PL 0006/4073
Tylasul Premix 100
PL 4188/4016
Uniprim 150
PL 4188/4011
Unizole S-For Pigs and Poultry
PL 2987/4004
Zinc Oxide Items shown in italics did not appear in the Schedule to S.I. 1990/2496.
Alternative product names used by specially authorised persons are not shown.

## Schedule 4 HORSE WORMERS

Product Licence No.
Name of Product
(a) Items shown in italics did not appear in the Schedule to S.I. 1990/2496.
(b) Alternative product names used by specially authorised persons are not shown.
PL 0010/4063
Bayverm Granules 10
PL 0010/4054
Bayverm LV Paste
PL 3636/4015
Dio Horse and Pony Wormer Paste
PL 5151/4001
Equidin Paste
PL 3832/4012
Equitac
PL 0025/4027
Equizole Pony Paste
PL 0025/4005
Equizole Powder
PL 0025/4042
Eqvalan Paste for Horses
PL 0844/4055
Multiwurma (Horses)
PL 0086/4107
Panacur 22% Granules
PL 0086/4119
Panacur Paste
PL 0086/4106
Panacur 10 Suspension
PL 1447/4094
Rycovet Horse and Pony Wormer Paste
PL 0057/4060
Strongid-P Granules
PL 0057/4062
Strongid-P Paste
PL 0286/4039
Synanthic Horse Paste
PL 5869/4061
Systamex Paste
PL 0242/4013
Telmin
PL 0242/4014
Telmin Paste

## Explanatory note

(This note is not part of the Order)
This Order revokes the Medicines (Veterinary Drugs) (Pharmacy and Merchants' List) (No. 2) Order 1989, as amended.
The Order continues to provide for certain exemptions from the restrictions imposed by section 52 of the Medicines Act 1968 (“the Act”). Section 52 restricts the retail sale or supply of medicinal products not on a general sale list (a general sale list being a list of medicinal products which are specified in an Order under section 51 of the Act and which may be freely sold) to sale or supply from a registered pharmacy by or under the supervision of a pharmacist.
The Order continues to exempt from section 52 the retail sale or supply of any veterinary drug described in article 3(1) by specified persons subject to certain conditions (article 3).
The Order continues to exempt from section 52 the placing on the market of any veterinary drug incorporated in an intermediate feed by specified persons subject to certain conditions (article 6).
Pursuant to article 2 of Council Directive 90/167/EEC (laying down the conditions governing the preparation, placing on the market and use of medicated feeding stuffs in the Community, OJ No. L 92, 7.4.90 p.42) a definition of “placing on the market” has been inserted in article 2(1) and the consequential amendments made to articles 6, 7, 8, 9 and 10 in respect of provisions governing intermediate feed. This amendment is made under the provisions of section 2(2) of the European Community Act 1972.
The Order also continues to exempt from section 52 the retail sale or supply of specified veterinary drugs for incorporation in animal feeding stuffs where the sale or supply is by specified persons subject to certain conditions (article 9).
Pursuant to article 4 of Council Directive 90/167/EEC the period of time that the record of any sale of veterinary drugs or intermediate feed is required to be kept pursuant to articles 4(3), 7(3) and 10(2) is extended from two to three years.
The Order also continues to exempt from section 52 the retail sale or supply of any veterinary drug (horse wormers) by specified persons subject to certain conditions (article 11).
Further exemptions continue to be given in respect of the retail sale or supply of specified drugs in a registered pharmacy by persons acting on behalf of a pharmacist and to the supply of specified drugs by a pharmacist subsequent to retail sale (article 13) and in cases involving another person’s default (article 14).
The fees for the registration, retention and restoration in the Register of Category 1 agricultural merchants (article 5(7)) and for saddlers (article 12(7)) have been slightly increased; the fees for the registration, retention and restoration in the Register of Category 2 agricultural merchants (article 8(7)) have been slightly decreased.
The Codes of Practice referred to in the Order have been updated and are priced publications available from MAFF Publication, London SE 997TP.

---
Source: https://www.legislation.gov.uk/uksi/1992/33 (the official version)
Page: https://openlegislation.uk/medicines-veterinary-drugs-pharmacy-and-merchants-list-order-1992
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.