# The Human Medicines Regulations 2012, Paragraph 25


The qualitative and quantitative composition, using the usual common name or chemical description, of the medicinal product in terms of—
(a) the active substances; and
(b) those excipients of which knowledge is essential for proper administration of the medicinal product.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/8/paragraph/25 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-8/paragraph-25
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.