
1 

(1) This Order may be cited as the Medicines (Products Other Than Veterinary Drugs) (Prescription Only) Amendment Order 1995 and shall come into force on 30th June 1995.
(2) In this Order “the principal Order” means the Medicines (Products Other Than Veterinary Drugs) (Prescription Only) Order 1983.
2 
In article 3(1)(a) of the principal Order (medicinal products on prescription only), for “Article 4(1) to (1V)” there is substituted “Article 4(1) to (1Z)”.
3 
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.
”
4 
In Part I of Schedule 1 to the principal Order (which lists substances which render a medicinal product a prescription only medicine except in the circumstances also listed)—
(a) the following substances are inserted at the appropriate points in the alphabetical order of the substances listed in Column 1:
 Azelastine Hydrochloride Lithium Succinate;
(b) in relation to the substance Pseudoephedrine Hydrochloride, for the entry “180mg (MDD)” at (a) and at (b) in Column 4, there is substituted in both places the entry “240mg (MDD)”.
5 
In Part III of Schedule 1 to the principal Order (medicinal products, specified by name and product licence number, that are prescription only medicines), the following entries are omitted:
 Ancoloxin 0021/5060 Debendox 0027/5001 Perstorp Dextrinomer Iodine 3863/0001.
6 
In Table A of Part IV of Schedule 1 to the principal Order, (medicinal products, specified by name and product licence number, that are not prescription only medicines),:
(a) the following entries are omitted:
 Anflam Cream 0142/0190 Anflam Cream 0.5% 0142/0263 Anflam Ointment 0142/0191 Anflam Ointment 0.5% 0142/0262 CP Hydrocortisone Cream 0.5% 4543/0238 CP Hydrocortisone Cream 1% 4543/0239 CP Hydrocortisone Ointment 0.5% 4543/0236 CP Hydrocortisone Ointment 1% 4543/0237 Dermacort Hydrocortisone 0129/0076 Efcortelan P Cream 0004/0327 Efcortelan P Ointment 0004/0326 Evacort Cream 0039/0198 Kerfoot Hydrocortisone Cream 1% 0058/0092 Medicort Cream 3920/0010 Wasp-Eze Hydrocortisone Cream 0232/0058 Wasp-Eze Hydrocortisone Ointment 0232/0059 Zenoxone Ointment 0181/0032;

(b) the following entries are inserted at the appropriate points in the alphabetical order of the medicinal products listed:
 Efcortelan Eczema Cream 10949/0234 Efcortelan Eczema Ointment 10949/0235 Proctocream HC 0036/0065.
Signed by authority of the Secretary of State for Health
Tom Sackville
Parliamentary Under Secretary of State
Department of Health
23rd May 1995John Redwood
Secretary of State for Wales
25th May 1995Fraser of Carmyllie
Minister of State, The Scottish Office
25th May 1995Sealed with the Official Seal of the Department of Health and Social Services for Northern Ireland on 23rd May 1995.
F. A. Elliott
Permanent Secretary
