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Regulation (EU) 2023/1182 of the European Parliament and of the Council of 14 June 2023 on specific rules relating to medicinal products for human use intended to be placed on the market in Northern Ireland and amending Directive 2001/83/EC (Text with EEA relevance) article 5 CELEX: 32023R1182 Specific rules for the labelling of medicinal products as referred to in Article 1(1)
Medicinal products as referred to in Article 1(1) shall bear an individual label that complies with the following requirements: (a) it shall be attached to the packaging of the medicinal product in a conspicuous place in such a way that it is easily visible, clearly legible, and indelible; it shall not in any way be hidden, obscured, detracted from, or interrupted by any other written or pictorial matter or any other intervening material; (b) it shall state the words ‘UK only’. |