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Labelling veterinary medicinal products retailed out of their original outer packaging
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16. (1) A person who retails a veterinary medicinal product that has been divided and is not in its original outer packaging shall—
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(a) provide a copy of the original data sheet in respect of the product supplied by the manufacturer with the product, or
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(b) label the product or ensure that it is labelled when retailed, with at least the following information:
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(i) the proprietary name of the product;
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(ii) the words “for animal treatment only”;
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(iii) the species to be treated;
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(iv) the manner of administration;
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(v) the dosage and duration of treatment;
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(vi) the name of the person to whom the product is retailed;
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(vii) the name and business address of the retailer;
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(viii) precautions regarding administration of the product and any withdrawal period;
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(ix) if applicable, special import licence information; and
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(x) any other information specified in regulations made by the Minister necessary to safeguard public and animal health and the environment.
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(2) A person who fails to comply with subsection (1) commits an offence and is liable on summary conviction to a class A fine.
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