7. [F1The entries or a] succinct statement of the entries (if any) in the summary of the product characteristics[F2, or in any equivalent summary published by the holder of a temporary authorisation,] relating to—
(a)adverse reactions, precautions and relevant contra-indications;
(b)dosage and method of use so far as relevant to the indications shown in the advertisement, and
(c)where this is not obvious, method of administration so far as relevant to those indications.
Textual Amendments
F1Words in Sch. 30 para. 7 substituted (E.W.S.) (1.10.2014) by The Human Medicines (Amendment) (No. 2) Regulations 2014 (S.I. 2014/1878), regs. 1, 29 and words in Sch. 30 para. 7 substituted (N.I.) (1.10.2014) by The Human Medicines (Amendment) (No. 2) Regulations 2014 (S.R. 2014/324), regs. 1(1), 29
F2Words in Sch. 30 para. 7 inserted (6.11.2020) by The Human Medicines (Coronavirus and Influenza) (Amendment) Regulations 2020 (S.I. 2020/1125), regs. 1(2), 33(4) and words in Sch. 30 para. 7 inserted (N.I.) (6.11.2020) by The Human Medicines (Coronavirus and Influenza) (Amendment) Regulations 2020 (S.R. 2020/349), regs. 1(2), 33(4)