Therapeutic Goods (Poisons Standard—June 2023) Instrument 2023
2Poisons available for human use only from or on the prescription or order of a specialist physician or a dermatologist
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2 Poisons available for human use only from or on the prescription or order of a specialist physician or a dermatologist
3 Poisons available only from or on the prescription or order of a medical practitioner approved or authorised under section 19 of the Act
4 Poisons available only from or on the order of a specialist physician
5 Poisons for which possession without authority is illegal
6 Poisons available for human use only from or on the prescription or order of a specialist physician
7 Poisons available for human use only from or on the prescription or order of a dermatologist
8 Poison available for initial treatment of a patient only if authorised by certain health practitioners
9 Poisons which must be stored in a locked container to prevent unauthorised access
Appendix E—First aid instructions for poisons
1 Standard statements for first aid instructions
2 Poisons information centre contact information in statements
3 First aid instructions for poisons
Appendix F—Warning statements and general safety directions for poisons
1 Warning statements
2 Safety directions—general
3 Poisons information centre contact information in statements
4 Poisons that must be labelled with warning statements and safety directions
Appendix G—Dilute preparations
1 Substances exempt at or below certain concentrations
Appendix H—Schedule 3 medicines permitted to be advertised
1 Schedule 3 medicines permitted to be advertised
Appendix I—Blank
Appendix J—Conditions for availability and use of certain poisons included in Schedule 7
1 Conditions for supply of certain poisons included in Schedule 7
Appendix K—Human medicines required to be labelled with a sedation warning
1 Human medicines required to be labelled with a sedation warning
Appendix L—Requirements for dispensing labels for medicines
1 General
2 Additional warning statements for certain human medicines
Appendix M—Additional controls or supply requirements for poisons included in Schedule 3 to allow them to be provided by a pharmacist
Index
Reader’s guide
Introduction
This instrument is made under paragraph 52D(2)(b) of the Therapeutic Goods Act 1989 (the Act), and is a compilation of decisions made under section 52D of the Act. This instrument should be read in conjunction with the Scheduling Policy Framework (the SPF) of the Australian Health Ministers’ Advisory Council. Further information on the scheduling amendments and the SPF can be viewed on the Therapeutic Goods Administration’s website (). Refer to section 6 for definitions of specific terms used in this document including “medicine” and “poison” (noting that the definition of poison includes medicine).