Paragraph 7 Prescription only relevant medicinal products

Changes not yet applied. Later legislation changes this provision in ways not yet written into the text below:

Sch 5, para 5 am by Medicines for Human Use (Marketing Authorisations Etc.) 2003 reg 2
Sch.5, para.5(1)(f)(g) added by Medicines for Human Use (Marketing Authorisation Etc.) 1998 reg.3(1)
Sch.5, para.5(2)(b) amended by Medicines for Human Use (Marketing Authorisation Etc.) 1998 reg.3(2)
Sch. 5 para. 9 inserted by Medicines for Human Use 2009 reg. 2
Sch.5, para 5 amended by Medicines for Human Use (Marketing Authorisations Etc.) 2000 reg 5
Sch. 5 para. 2 words substituted by Medicines (Codification Amendments Etc.) 2002 reg. 8(i)(i)
Sch. 5 para. 2 words substituted by Medicines (Codification Amendments Etc.) 2002 reg. 8(i)(ii)
Sch 5, para 6 am by Medicines for Human Use and Medical Devices (Fees and Miscellaneous Amendments) 2002 reg 3(1), (6)

Subject to the following provisions of this Schedule, every container and every package immediately enclosing a container of a relevant medicinal product which is subject to restrictions imposed under section 58(1) of the Act (relevant medicinal products on prescription only) shall, if the product is described in heads (d) or (e) of sub-paragraph (2) of paragraph 6, be labelled to show the words and particulars set out in that head and shall, except where the product is sold by retail or supplied in circumstances corresponding to retail sale or is the subject of an exemption, by virtue of the provisions of section 58(4)(a), from any of the restrictions imposed by section 58(2) of the Act, be labelled to show the letters “POM” in capital letters within a rectangle within which there shall be no other matter of any kind.