# The Veterinary Medicines Regulations 2013, Paragraph 22: Labelling

Extent: E+W+S

(1) The holder of an authorisation under paragraph 14 must ensure that every container used is labelled with—
(a) a precise description of the product;
(b) the date on which the product was produced;
(c) the name and address of the authorisation holder;
(d) the address of the site named under the authorisation and its authorisation number;
(e) the instructions for use;
(f) the expiry date;
(g) any necessary warnings;
(h) in the case of an autogenous vaccine or an unauthorised veterinary medicinal product for administration under the cascade, the name of the veterinary surgeon who ordered the product;
(i) in the case of blood or a stem cell product—
(i) the identification of the donor animal; and
(ii) the date of collection.
(2) In the case of blood or blood constituents there must be no specific therapeutic indication on the label or on any information related to the product.
(3) In the case of an unauthorised veterinary medicinal product for administration under the cascade the words “this veterinary medicinal product does not hold a marketing authorisation” must appear on the label.

---
Source: https://www.legislation.gov.uk/uksi/2013/2033/schedule/2/paragraph/22 (the official version)
Page: https://openlegislation.uk/veterinary-medicines-regulations-2013/schedule-2/paragraph-22
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.