In article 4 of the principal Order (medicinal products that are not prescription only), the following paragraphs are inserted after paragraph (1V):—
(1W) Notwithstanding article 3(1)(a), a medicinal product shall not be a prescription only medicine by reason that it consists of or contains the substance fluconazole where—
(a) the medicinal product is indicated for oral administration for the treatment of vaginal candidiasis in persons aged not less than 16 nor more than 60 years;
(b) it is sold or supplied in a container or package containing not more than 150 milligrams of the medicinal product; and
(c) the container or package is labelled to show a maximum dose of 150 milligrams of fluconazole.
(1X) Notwithstanding article 3(1)(a), a medicinal product shall not be a prescription only medicine by reason that it contains the substance hydroxyzine hydrochloride where—
(a) the medicinal product is indicated for the management of pruritus associated with acute or chronic urticaria or atopic dermatitis or contact dermatitis, in adults and in children aged not less than 6 years;
(b) it is sold or supplied in a container or package containing not more than 750 milligrams of the medicinal product; and
(c) the container or package is labelled to show a maximum dose of 25 milligrams and a maximum daily dose of 75 milligrams in the case of adults and in children aged not less than 12 years and a maximum daily dose of 50 milligrams in the case of children aged not less than 6 nor more than 12 years.
(1Y) Notwithstanding article 3(1)(a), a medicinal product shall not be a prescription only medicine by reason that it contains the substance ketoconazole where—
(a) the medicinal product is in the form of a shampoo;
(b) the maximum strength of the ketoconazole in the medicinal product does not exceed 2 per cent. calculated in terms of weight in weight;
(c) the medicinal product is indicated for the prevention and treatment of dandruff and seborrhoeic dermatitis of the scalp;
(d) it is sold or supplied in a container or package containing not more than 120 millilitres of the medicinal product, containing not more than 2400 milligrams of ketoconazole; and
(e) the container or package is labelled to show a maximum frequency of application of once every 3 days.
(1Z) Notwithstanding article 3(1)(a), a medicinal product shall not be a prescription only medicine by reason that it consists of or contains the substance pyrantel embonate where—
(a) the medicinal product is indicated for the treatment of enterobiasis, in adults and in children aged not less than 2 years;
(b) it is sold or supplied in a container or package containing not more than 750 milligrams of the medicinal product; and
(c) the container or package is labelled to show a maximum daily dose (to be taken as a single dose) of pyrantel embonate of 750 milligrams in the case of adults and children aged not less than 12 years, of 500 milligrams in the case of children aged not less than 6 nor more than 12 years and of 250 milligrams in the case of children aged not less than 2 nor more than 6 years.