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Regulation (EC) No 1272/2008 of the European Parliament and of the CouncilShow full title

Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006 (Text with EEA relevance)

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There are currently no known outstanding effects by UK legislation for Regulation (EC) No 1272/2008 of the European Parliament and of the Council, Article 36. Help about Changes to Legislation

Article 36U.K. [F1Mandatory] classification and labelling of substances

1.A substance that fulfils the criteria set out in Annex I for the following shall normally be subject to [F2mandatory] classification and labelling in accordance with Article 37 [F3or Article 37A]:

(a)respiratory sensitisation, category 1 (Annex I, section 3.4);

(b)germ cell mutagenicity, category 1A, 1B or 2 (Annex I, section 3.5);

(c)carcinogenicity, category 1A, 1B or 2 (Annex I, section 3.6);

(d)reproductive toxicity, category 1A, 1B or 2 (Annex I, section 3.7).

2.A substance that is an active substance in the meaning of [F4Regulation (EC) No 1107/2009 or Regulation (EC) No 528/2012] shall normally be subject to [F5mandatory] classification and labelling. For such substances, the procedures set out in Article 37 [F6or Article 37A], F7... shall apply.

3.Where a substance fulfils the criteria for other hazard classes or differentiations than those referred to in paragraph 1 and does not fall under paragraph 2, a [F8mandatory] classification and labelling [F9requirement] in accordance with Article 37 [F10or Article 37A] may also be added to [F11the GB mandatory classification and labelling list] on a case-by-case basis, if justification is provided demonstrating the need for such action F12....

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