Paragraph 2

In this Schedule—

• “2012 Regulations” means the Human Medicines Regulations 2012^f1;

• “aerodrome security restricted area” means a security restricted area designated by the Secretary of State for the purposes of section 11A of the Aviation Security Act 1982^f2;

• “box” includes a crate or other containers of a similar nature;

• “listed appliance” means a listed appliance within the meaning of section 27 of the National Health Service (Scotland) Act 1978^f3;

• “medicinal product” has the same meaning as in section 130 of the Medicines Act 1968 Act^f4;

• “pharmacy medicine” means a medicinal product, other than a prescription only medicine, that—

  1. (a)

     in accordance with regulation 220 of the 2012 Regulations, can only be sold or supplied under the conditions specified in paragraph (2)(a) to (c) of that regulation; or

  2. (b)

     but for the fact that it is sold or supplied in accordance with regulation 223 of those Regulations^f5, could only be lawfully sold or supplied under those conditions;

• “prescription” means a prescription issued by—

  1. (a)

     a registered medical practitioner;

  2. (b)

     a person registered in the dentists register kept under section 14 of the Dentists Act 1984^f6;

  3. (c)

     an EEA health professional, as defined in regulation 213(1) of the 2012 Regulations^f7;

  4. (d)

     a nurse independent prescriber, as defined in regulation 8(1) of the 2012 Regulations;

  5. (e)

     an optometrist independent prescriber, as defined in regulation 8(1) of the 2012 Regulations;

  6. (f)

     a pharmacist independent prescriber, as defined in regulation 8(1) of the 2012 Regulations; or

  7. (g)

     a supplementary prescriber, as defined in regulation 8(1) of the 2012 Regulations;

• “prescription only medicine” has the same meaning as in regulation 5(3) of the 2012 Regulations; and

• “unpackaged” means wholly or partly unwrapped.