2002 No. 3170
The Medicines for Human Use (Kava-kava) (Prohibition) Order 2002
Made
Laid before Parliament
Coming into force
As respects England, Wales and Scotland, the Secretary of State concerned with health in England and as respects Northern Ireland, the Department of Health, Social Services and Public Safety, acting jointly, in exercise of the powers conferred upon them by section 62(1)(a) and (2) of the Medicines Act 1968M1 or, as the case may be, the powers conferred by those provisions and now vested in themM2, and of all other powers enabling them in that behalf, it appearing to them to be necessary in the interests of safety to make the following Order, after consulting such organisations as appear to them to be representative of interests likely to be substantially affected by the Order pursuant to section 129(6) of that Act, after consulting and taking into account the advice of the Committee on Safety of Medicines pursuant to sections 62(3) and 129(7) of that ActM3, and after taking into account the report of the Medicines Commission made under section 62(5) of that Act, hereby make the following Order:
In the case of the Secretary of State concerned with health in England, by virtue of article 2(2) of, and Schedule 1 to, S.I. 1969/388, and articles 2(1) and 5 of, and paragraph 1(1) of the Schedule to, S.I. 1999/3142; and in the case of the Department of Health, Social Services and Public Safety, the powers vested in the Minister in charge of that Department by virtue of section 95(5) of, and paragraph 10 of Schedule 12 to the Northern Ireland Act 1998 (c.47) may now be exercised by the Department by virtue of section 1(8) of, and paragraph 4(1)(b) of the Schedule to, the Northern Ireland Act 2000 (c.1); the Department was renamed by virtue of Article 3(6) of S.I. 1999/283 (N.I.1).
Section 62(3) refers to the “appropriate committee”, which is defined in section 4(6) of the Act. The Committee on Safety of Medicines was established under section 4 of the Act, by S.I. 1970/1257, for the purposes set out in that instrument.
Citation, commencement and interpretation1
1
This Order may be cited as the Medicines for Human Use (Kava-kava) (Prohibition) Order 2002 and shall come into force on 13th January 2003.
2
In this Order—
“the Act” means the Medicines Act 1968;
“EEA Agreement” means the Agreement on the European Economic Area signed at Oporto on 2nd May 1992 M4 as adjusted by the Protocol signed at Brussels on 17th March 1993 M5;
“EEA State” means a State which is a Contracting Party to the EEA Agreement;
“external use” means application to the skin, hair, teeth, mucosa of the mouth, throat, nose, ear, eye, vagina or anal canal when a local action only is intended and extensive systemic absorption is unlikely to occur, and references to medicinal products being “for external use” shall be read accordingly—except that such references shall not include throat sprays, throat pastilles, throat lozenges, throat tablets, nasal drops, nasal sprays, nasal inhalations or teething preparations;
“free circulation in member States” has the same meaning as in Article 23.2, as read with Article 24, of the Treaty establishing the European Community; and
“medicinal product” does not include a medicinal product which is a veterinary drug.
Prohibition of sale, supply and importation of any medicinal product consisting of or containingPiper methysticum (known as Kava-kava)2
Subject to article 3 below, the sale, supply or importation of any medicinal product consisting of or containing—
a
a plant M6 belonging to the speciesPiper methysticum (known as Kava-kava); or
b
an extract from such a plant,
is prohibited.
Exceptions to the prohibition imposed by article 23
The prohibition imposed by article 2 above shall not apply where the medicinal product is—
a
for external use only;
b
sold or supplied to, or is imported by or on behalf of, any of the following persons—
i
ii
iii
a person duly authorised by an enforcement authority under sections 111 and 112 of the Act, or
iv
a sampling officer within the meaning of Schedule 3 to the Act M11;
c
imported from an EEA State, if the product—
i
originates in an EEA State, or
ii
originates outside the European Economic Area, but is in free circulation in member States,
and is being, or is to be, exported to an EEA State other than the United Kingdom; or
d
the subject of—
i
a product licence M12,
ii
a marketing authorization within the meaning given in regulation 1(4)(a) of the Medicines for Human Use (Marketing Authorisation Etc.) Regulations 1994 M13, or
iii
F2iv
a traditional herbal registration within the meaning given in regulation 2(1) of the Medicines (Traditional Herbal Medicinal Products for Human Use) Regulations 2005.
Signed by authority of the Secretary of State for Health
Sealed with the Official Seal of the Department of Health, Social Services and Public Safety
1968 c.67; the expression “the appropriate Ministers” and the expression “the Health Ministers”, which are relevant to the powers being exercised in the making of this Order, are defined in section 1 of that Act, as amended by article 2(2) of, and Schedule 1 to, S.I. 1969/388 and by article 5 of, and paragraph 1(1) of the Schedule to, S.I. 1999/3142.