# The Human Medicines Regulations 2012, Regulation 257AB: Transitional arrangements


The information specified in paragraph 18B of Schedule 24 is not required to appear on the packaging of a medicinal product released for sale or distribution before 1st January 2025, unless the product has been re-packaged or relabelled after that date.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/regulation/257AB (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/regulation-257AB
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.