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Art. 10 Labelling
1 Manufacturers making available or supplying dangerous substances or preparations to third parties must label them in accordance with the following provisions:
2 Preparations with particular hazards referred to in Article 4 paragraph 7 of the CLP Regulation must additionally be labelled in accordance with Article 25 paragraph 6 of the CLP Regulation. 3 In addition to paragraphs 1 and 2, the labelling must meet the following requirements:
3bis In the case of substances or preparations imported from a member state of the EEA, the manufacturer’s name may be replaced on the labelling by the name of the person responsible for placing on the market in the EEA, if the substances or preparations:44
4 If further label elements are required in order to comply with other legislation, these are to be included in the section for supplemental information in accordance with Article 25 of the CLP Regulation. 5 Where the name in the IUPAC nomenclature46 exceeds 100 characters, another name may be used, provided that the report in accordance with Article 49 includes both the name given in the IUPAC nomenclature and the other name used. 6 The requirements of paragraph 1 are deemed to have been met if the inner packaging is labelled before the application of or immediately after the removal of the transport packaging. Responsibility for packaging and labelling rests with the manufacturer. 40 The correction of 24 April 2023 relates to the French and Italian texts only (AS 2023 193). 41 See footnote to Art. 2 para. 4. 42 Amended by No I of the O of 11 March 2022, in force since 1 May 2022 (AS 2022 220). 43 Amended by No I of the O of 31 Jan. 2018, in force since 1 March 2018 (AS 2018 801). 44 Amended by No I of the O of 11 March 2022, in force since 1 May 2022 (AS 2022 220). 45 Inserted by No I of the O of 31 Jan. 2018, in force since 1 March 2018 (AS 2018 801). 46 Chemical nomenclature of the International Union of Pure and Applied Chemistry (IUPAC): www.iupac.org |