SCHEDULE 1Further provisions for classification of medicinal products
PART 1Descriptions of certain medicinal products to be available only on prescription
1.
The following medicinal products shall be available only on prescription—
(a)
a product for parenteral administration;
(b)
a product that is a controlled drug F1as defined in section 2(1)(a) of the Misuse of Drugs Act 1971, unless it is covered by a marketing authorisation in which the product is classified as a pharmacy medicine or as a medicinal product subject to general sale;
(c)
cyanogenic substances, other than preparations for external use;
(d)
medicinal substances that on administration emit radiation, or contain or generate any substance which emits radiation, in order that radiation may be used;
(e)
a product that—
(i)
is covered by a marketing authorisation in which the product is classified as a pharmacy medicine or as a medicinal product subject to general sale, and
(ii)
consists of or contains aloxiprin, aspirin or paracetamol in the form of non-effervescent tablets or capsules;
(f)
a product that—
(i)
is covered by a marketing authorisation in which the product is classified as a pharmacy medicine or as a medicinal product subject to general sale, and
(ii)
consists of or contains (in any pharmaceutical form) pseudoephedrine salts or ephedrine base or salts; and
(g)
a product that—
(i)
is not covered by a marketing authorisation, and
(ii)
is a prescription only medicine by virtue of articles 5 and 10 of, and Schedules 1 and 2 to, the Prescription Only Medicines (Human Use) Order 1997 M1.