Changes between two versions
What changed between the adopted text of 4 Oct 2023 and the adopted text of 23 Apr 2024
From · adopted text· 4 Oct 2023
Classification, labelling and packaging of substances and mixtures
To · adopted text· 23 Apr 2024
Classification, labelling and packaging of substances and mixtures
These two texts have too little in common to compare paragraph by paragraph: they are different documents rather than versions of one (for example one group’s motion and the joint text that was adopted).
+16 added · −174 removed · 1 changed paragraphs, packaging included.
Part 4 of 4: Paragraphs 181–195
Removed:Annex I – paragraph 1 – point -1 (new), Annex I – Part 1 – Section 1.5.2.4.1. – point b – point v a (new): (va) Skin sensitisation, category 1 (sub-categories 1A and 1B);
Removed:Regulation (EC) No 1272/2008
Removed:Annex II – paragraph 1 – point -1 a(new), Annex II – Part 3 – Section 3.1.1.1: -1a in Part 3 of Annex II to Regulation (EC) No 1272/2008, point 3.1.1.1. is amended as following: / "3.1.1.1. Packaging of whatever capacity containing a substance or mixture supplied to the general public and classified for acute toxicity, categories 1 to 3, STOT — single exposure category 1, STOT — repeated exposure category 1, or skin corrosion category 1, or serious eye damage category 1 shall be fitted with child-resistant fastenings."
Removed:Regulation (EC) No 1272/2008
Removed:Annex II – paragraph -1 a (new), Annex II – Part 3 – section 3.2.1: (-1a) In Part 3 of Annex II, section 3.2.1. is replaced by the following: / "3.2.1. Packaging to be fitted with a tactile warning / Where substances or mixtures are supplied to the general public and classified for acute toxicity, skin corrosion/skin irritation, serious eye damage/eye irritation, endocrine disruption for human health category 2, endocrine disruption for the environment category 2, germ cell mutagenicity category 2, carcinogenicity category 2, reproductive toxicity category 2, respiratory or skin sensitization, STOT categories 1 or 2, aspiration hazard, flammable gases, flammable liquids categories 1 or 2, or flammable solids, the packaging of whatever capacity, shall be fitted with a tactile warning of danger. "
Removed:Regulation (EC) No 1272/2008
Removed:Annex II – paragraph 1 – point 1, Annex II – Part 3 – Section 3.4 – point b: (b) a label is firmly affixed on a visible place of the refill station and fulfils the requirements of Article 31;
Removed:Regulation (EC) No 1272/2008
Removed:Annex II – paragraph 1 – point 1, Annex II – Part 3 – Section 3.4 – point b a (new): (ba) a label is available at the refill station, free-of-charge for consumers in a self-adhesive sticker form to be affixed on the container used by the consumer. Where refill stations provide several substances or mixtures, labels should easily and clearly identify which substance or mixture provided at the refill station the labels correspond to;
Removed:Regulation (EC) No 1272/2008
Removed:Annex II – paragraph 1 – point 1, Annex II – Part 3 – Section 3.4. – point k – point iv a (new): (iva) Serious eye damage category 1/eye irritation, category 2;
Removed:Regulation (EC) No 1272/2008
Removed:Annex II – paragraph 1 – point 1, Annex II – Part 3 – Section 3.4. – point k – point v a (new): (va) Skin sensitisation, category 1 (sub-categories 1A and 1B);
Removed:Regulation (EC) No 1272/2008
Removed:Annex III – paragraph 1 a (new), Annex VI: Annex VI is amended as follows: / "ANNEX VI / — Justification for the proposed grouping of substances to harmonized classification and labelling. / Where a harmonised classification and labelling proposal is made for a group of substances, the dossier shall include a scientific justification. / — Justification for other effects at Community level / For effects other than carcinogenity, mutagenicity, reprotoxicity, endocrine disruption for human health and the environment, persistent bioaccumulative and toxic (PBT), very persistent, very bioaccumulative (vPvB), persistent, mobile and toxic (PMT), very persistent, very mobile (vPvM), and respiratory sensitisation, a justification that there is a need for action demonstrated at Union level shall be provided. This will not apply for an active substance within the meaning of Regulation (EU) No 1107/2009 or Regulation (EU) No 528/2012."