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Therapeutic Goods Order No. 69 - General requirements for labels for medicines (27/08/2001)
No longer in force
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Administered by
Department of Health, Disability and Ageing
This item is authorised by the following title:
Therapeutic Goods Act 1989
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F2014C00926
12 June 2014
-
30 June 2017
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General requirement for labels for medicines
Introduction
1 Application and exemptions
2 Interpretation
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3 Label requirements
3(1) General
3(2) Particulars to be included on a label
3(3) Particulars to be included on a main label
3(4) Preparations for ophthalmic use
3(5) Injections other than large volume injections
3(6) Large volume injections
3(7) Dialysis concentrates
3(8) Peritoneal dialysis solutions
3(9) Preparations for use on skin or mucous membranes
3(10) Biological products
3(11) Small containers
3(12) Individually wrapped goods
3(13) Strip, blister and dial dispenser packs
3(14) Directions for use
3(15) Homoeopathic preparations
3(16) Formulations containing both homoeopathic and non-homoeopathic ingredients
3(17) Plastic ampoules
3(18) Composite packs
4 Expression of quantity or proportion of active ingredient in medicines
5 Expression of potency in biological products
6 Expression of activity of radionuclides in radiopharmaceutical preparations
7 Permitted statements of storage conditions
First schedule
Second schedule
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Endnotes
Endnote 1—About the endnotes
Endnote 2—Abbreviation key
Endnote 3—Legislation history
Endnote 4—Amendment history
Endnote 5—Uncommenced amendments [none]
Endnote 6—Modifications [none]
Endnote 7—Misdescribed amendments [none]
Endnote 8—Miscellaneous [none]
