(1) In article 4 of the principal Order (medicinal products that are not prescription only), for paragraph (1C), there is substituted the following paragraph:—
(1C) Notwithstanding article 3(1)(a), a medicinal product shall not be a prescription only medicine by reason that it contains the substance mebendazole where—
(a) the medicinal product is indicated for oral use in the treatment of enterobiasis in adults and in children over the age of 2 years;
(b) its container or package is labelled to show a maximum dose of 100 milligrams of mebendazole; and
(c) it is sold or supplied in a container or package containing not more than 400 milligrams of mebendazole.
(2) In article 4 of the principal Order the following paragraphs are inserted after paragraph (1J):—
(1K) Notwithstanding article 3(1)(a), a medicinal product shall not be a prescription only medicine by reason that it contains the substance beclomethasone dipropionate where—
(a) the medicinal product is indicated only for the treatment of seasonal allergic rhinitis by non-aerosol nasal administration, in adults and in children over the age of 12 years;
(b) it is sold or supplied in a container or package containing not more than 200 doses; and
(c) its container or package is labelled to show a maximum dose of 100 micrograms per nostril and a maximum daily dose of 200 micrograms per nostril of beclomethasone dipropionate.
(1L) Notwithstanding article 3(1)(a), a medicinal product shall not be a prescription only medicine by reason that it contains the substance cimetidine where—
(a) the medicinal product is indicated for the short-term symptomatic relief of heartburn, dyspepsia and hyperacidity; and
(b) its container or package is labelled to show a maximum dose of 200 milligrams and a maximum daily dose of 800 milligrams of cimetidine for a maximum period of 14 days.
(1M) Notwithstanding article 3(1)(a), a medicinal product shall not be a prescription only medicine by reason that it contains the substance cimetidine where—
(a) the medicinal product is for the prophylactic management of nocturnal heartburn; and
(b) its container or package is labelled to show a maximum dose of 100 milligrams of cimetidine to be taken once daily at night for a maximum period of 14 days.
(1N) Notwithstanding article 3(1)(a), a medicinal product shall not be a prescription only medicine by reason that it contains the substance famotidine where—
(a) the medicinal product is indicated for the short-term symptomatic relief of heartburn, dyspepsia and hyperacidity; and
(b) its container or package is labelled to show a maximum dose of 10 milligrams and a maximum daily dose of 20 milligrams of famotidine for a maximum period of 14 days.
(1O) Notwithstanding article 3(1)(a), a medicinal product shall not be a prescription only medicine by reason that it contains the substance sodium cromoglycate where—
(a) the medicinal product is indicated for the treatment of acute seasonal allergic conjunctivitis;
(b) it is in the form of aqueous eye drops;
(c) the maximum strength of the sodium cromoglycate in the medicinal product does not exceed two per cent. calculated in terms of weight in volume; and
(d) it is sold or supplied in a container containing not more than 10 millilitres of the medicinal product.
(1P) Notwithstanding article 3(1)(a), a medicinal product shall not be a prescription only medicine by reason that it contains the substance sodium cromoglycate where—
(a) the medicinal product is indicated for the treatment of acute seasonal allergic rhinitis;
(b) it is in the form of an eye ointment;
(c) the maximum strength of the sodium cromoglycate in the medicinal product is four per cent. calculated in terms of weight in weight; and
(d) it is sold or supplied in a container or package containing not more than 5 grams of the medicinal product.