Therapeutic Goods (Restricted and Prohibited Representations - Nicotine) Permission (No. 2) 2021
I, John Skerritt, as delegate of the Secretary of the Department of Health, make the following permission.
Dated 17 August 2021
Adjunct Professor John Skerritt
Health Products Regulation Group
Department of Health
Schedule 2 - Repeals - Therapeutic Goods (Restricted and Prohibited Representations - Nicotine) Permission 2021
This instrument is the Therapeutic Goods (Restricted and Prohibited Representations - Nicotine) Permission (No. 2) 2021.
- Each provision of this instrument specified in column 1 of the table commences, or is taken to have commenced, in accordance with column 2 of the table. Any other statement in column 2 has effect according to its terms.
|Column 1||Column 2||Column 3|
|1. The whole of this instrument||The day after this instrument is made.||18 August 2021|
Note: This table relates only to the provisions of this instrument as originally made. It will not be amended to deal with any later amendments of this instrument.
- Any information in column 3 of the table is not part of this instrument. Information may be inserted in this column, or information in it may be edited, in any published version of this instrument.
This instrument is made under section 42DK of the Therapeutic Goods Act 1989.
Note: A number of expressions used in this instrument are defined in subsection 3(1) of the Act, including the following:
(b) current Poisons Standard;
(c) included in the Register;
(d) medical device;
(g) therapeutic goods;
(h) Therapeutic Goods Advertising Code.
In this instrument:
Act means Therapeutic Goods Act 1989.
established nicotine replacement therapy means a therapeutic good that is included in the Register, other than a nicotine vaping product, that:
- contains nicotine as the only active ingredient; and
- has an indication accepted in relation to its inclusion that relates to assisting with smoking cessation.
nicotine vaping product has the same meaning as in TGO 110 and includes both a product that is, and a product that is not, included in the Register.
Note 1: Nicotine vaping product is defined in section 4 of TGO 110 to mean a medicine that contains nicotine in solution and that is:
(a) a finished product; and
(b) intended to be vaporised and administered by inhalation using a vaping device.
Note 2: Nicotine vaping products may also be described as nicotine vape liquids, or nicotine e-liquids.
Note 3: Examples of vaping devices include e-cigarettes, e-cigars, e-hookah pens, e-pens, e-pipes and vape pens.
Note 4: A nicotine vaping product that is not included in the Register has not been evaluated by the Secretary under section 25 of the Act for quality, safety and efficacy.
prohibited representation means a representation referred to in subsection 42DJ(1) of the Act.
relevant person means a retail pharmacy or a pharmacy marketing group.
Note: A reference to a community pharmacy includes a reference to an online pharmacy.
restricted representation means a representation referred to in section 42DD of the Act.
TGO 110 means the Therapeutic Goods (Standard for Nicotine Vaping Products) (TGO 110) Order 2021.
Note: TGO 110 is a legislative instrument published on the Federal Register of Legislation.
trade name has the same meaning as in the Therapeutic Goods Regulations 1990.
- For subsection 42DK(1) of the Act, in relation to each item mentioned in the table in Schedule 1, the representations specified in column 2 (to the extent that those representations are restricted representations) are permitted to be used in the advertisements specified in column 3, about the therapeutic goods specified in column 4, subject to the conditions (if any) specified in column 5.
- For subsection 42DK(3) of the Act, in relation to each item mentioned in the table in Schedule 1, the representations specified in column 2 (to the extent that those representations are prohibited representations) are permitted to be used in the advertisements specified in column 3, about the therapeutic goods specified in column 4, subject to the conditions (if any) specified in column 5.
- To avoid doubt, a reference in an advertisement that is made in accordance with this instrument, relating to therapeutic goods containing a substance included in Schedule 3, 4 or 8 to the current Poisons Standard or therapeutic goods that are not included in the Register, is by virtue of this instrument also authorised by the Australian Government Department of Health for the purposes of subsections 42DL(10) and (12), and 42DLB(7) and (9), of the Act.
Each instrument that is specified in Schedule 2 is repealed as set out in the applicable items in that Schedule.
Schedule 1 - Permission
Note: See section 5.
|Column 1||Column 2||Column 3||Column 4||Column 5|
a representation that is:
but may be modified in accordance with one or more of the following:
an advertisement about the therapeutic goods made by the relevant person mentioned in column 2, through one or more of the following media under the direct control of that person:
a nicotine vaping product, and any associated vaping device that is a medical device used exclusively for the vaporisation and administration by inhalation of the nicotine vaping product
the advertisement must not:
a representation to the effect that the therapeutic goods assist with smoking cessation
|an advertisement about the therapeutic goods||an established nicotine replacement therapy|
Note 1: The evidence relating to nicotine vaping products assisting with smoking cessation is mixed.
Note 2: The advertisements mentioned in items 1 and 2 of the table in Schedule 1 must comply with the Act and the Therapeutic Goods Advertising Code, including requirements relating to the accuracy of the advertisements and the use of mandatory warning statements.
Note: See section 6.
Therapeutic Goods (Restricted and Prohibited Representations - Nicotine) Permission 2021
1 The whole of the instrument
Repeal the instrument.