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The Human Medicines Regulations 2012, Section 102 is up to date with all changes known to be in force on or before 05 November 2024. There are changes that may be brought into force at a future date. Changes that have been made appear in the content and are referenced with annotations.
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102.—(1) This Part applies to a homoeopathic medicinal product (a “registrable homoeopathic medicinal product”) that meets the following conditions.
(2) Condition A is that the product is administered orally or externally.
(3) Condition B is that no specific therapeutic indication appears—
(a)on the labelling of the product; or
(b)in any information supplied with the product.
(4) Condition C is that—
(a)the product contains no more than one part per 10,000 of the mother tincture; and
(b)in a case where the product's active substance is a relevant allopathic substance, the product contains no more than 1/100th of the smallest concentration of that substance used in allopathy.
(5) In this regulation “relevant allopathic substance” means an active substance whose presence in an allopathic medicinal product means that the product is only available on prescription.
(6) For this purpose—
(a)“allopathic medicinal product” means a medicinal product other than a homoeopathic medicinal product; and
(b)“allopathy” means treatment using an allopathic medicinal product.
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