1998 No. 1178
The Prescription Only Medicines (Human Use) Amendment (No. 2) Order 1998
Made
Laid before Parliament
Coming into force
except for article 2(d)(ii)
article 2(d)(ii)
The Secretaries of State concerned with health in England, in Wales and in Scotland respectively and the Department of Health and Social Services for Northern Ireland, acting jointly, in exercise of powers conferred on them by sections 58(1), (4) and (5) and 129(4) of the Medicines Act 19681 or, as the case may be, those conferred by the said provisions and now vested in them2, and of all other powers enabling them in that behalf, after consulting such organisations as appear to them to be representative of interests likely to be substantially affected by this Order, pursuant to section 129(6) of that Act, and after consulting and taking into account the advice of the Medicines Commission pursuant to sections 58(6) and 129(7) of that Act, hereby make the following Order:
Citation, commencement and interpretation1
1
This Order may be cited as the Prescription Only Medicines (Human Use) Amendment (No. 2) Order 1998 and shall come into force on 1st June 1998, except for article 2(d)(ii) which shall come into force on 16th September 1998.
2
In this Order “the principal Order” means the Prescription Only Medicines (Human Use) Order 19973.
Amendment of Schedule 1 to the principal Order2
In Schedule 1 to the principal Order (which specifies substances which when included in medicinal products make those products prescription only medicines and exemptions from restrictions on the sale and supply of prescription only medicines)—
a
in relation to the substance Domperidone Maleate, there are inserted the following entries—
in column 3
For the relief of post-prandial symptoms of excessive fullness, nausea, epigastric bloating and belching, occasionally accompanied by epigastric discomfort and heartburn,
in column 4
10mg (MD)
40mg (MDD)
and in column 5
Container or package containing not more than 100mg of Domperidone as Domperidone Maleate;
- a
in relation to the substance Minoxidil, there are substituted for the entry in column 2 the entries—
1
2.0 per cent
2
5.0 per cent
- a
and for the entry in column 3 the entries—
1
External
2
External use for the treatment of alopecia androgenetica, in men aged 18 to 65 (but not in women);
- a
in relation to the substance Nizatidine—
- i
there are inserted in the entry in column 3, after the word “prevention”, the words “and treatment”, and after the word “heartburn”, the words “and meal-induced indigestion”,
- ii
there is inserted in column 4, after the entry “75mg (MD)”, the entry “150mg (MDD)”, and
- iii
there is substituted in column 4 for the entry “Maximum of 4 such doses in any period of 14 days”, the entry “For a maximum period of 14 days”; and
- i
- b
there is inserted in column 1, at the appropriate point in the alphabetical order of the entries in that column, each of the following substances—
- i
“Pirenzepine Dihydrochloride Monohydrate”
- i
“Quinapril Hydrochloride” and
- ii
“Phenolphthalein.”
- ii
- a
Amendment of Schedule 5 to the principal Order3
In Part III of Schedule 5 to the principal Order there is inserted in the entry in column 2 of paragraph 9, after the words “Anhydrous Glucose”, the words “Bretylium Tosylate”.
Signed by the authority of the Secretary of State for Health
Sealed with the Official Seal of the Department of Health and Social Services for Northern Ireland on
(This note is not part of the Order)