Medicines Advisory Statements Specification 2016
4Definitions
Start here
Get a plain-English read of 4
Turn the raw legal text into a practical explanation grounded in Medicines Advisory Statements Specification 2016.
4 Definitions
(1) In this Specification:
Act means the Therapeutic Goods Act 1989
dermal use means application to the skin primarily for localised effect
divided preparation means a preparation manufactured and packed as discrete pre-measured dosage units prior to sale or supply, and includes tablets, capsules, cachets, single dose powders or single dose sachets of powders or granules
dosage unit means an individual dose of a medicine for therapeutic use and includes a tablet, capsule, cachet, single dose powder or single dose sachet of powders or granules
essential oils means products obtained from natural raw materials either by distillation with water or steam or from the epicarp of citrus fruits by a mechanical process, or by dry distillation. It also means:
(a) oils of equivalent composition derived through synthetic means; or
(b) compounded oils of equivalent composition comprising a mixture of synthetic and natural components
external in relation to the use of a medicine means application in the ears, eyes or nose or to a body surface other than in the mouth, rectum, vagina, urethra or other body orifice
internal use means administration:
(a) orally, except for topical effect in the mouth; or
(b) for absorption and the production of a systemic effect,
(i) by way of a body orifice other than the mouth; or
(ii) parenterally, other than by application to unbroken skin
Labelling Order means the order in force made under section 10 of the Act and published on the Federal Register of Legislative Instruments, specifying general requirements for labelling of medicines
listed medicine means a medicine that is listed in the Register under sections 26 or 26A of the Act
main label means:
(a) where there are two or more labels or two or more portions of a single label – that label or portion of the label where the product name is more or most conspicuously shown; or
(b) where the product name is equally conspicuous on two or more labels or portions of a label –each such label or portion.
medicine has the same meaning as in the Act
medicine in a prescribed class means medicine in a class prescribed in the Regulations for the purposes of paragraph 3(5)(ca) of the Act
MRDD (Maximum recommended daily dose) is the maximum approved dose per day for a medicine used for its main indication in adults
Regulations means the Therapeutic Goods Regulations 1990
signal heading means the signal word or words relating to the Schedule of the SUSMP in which the substance is included and the purpose for which it is to be used, as shown in the following table: