1.

From the date on which an active substance is approved, the following up-to-date information held by the Agency or the Commission on active substances shall be made publicly and easily available free of charge: where available, the ISO name and the name in the International Union of Pure and Applied Chemistry (IUPAC) nomenclature; if applicable, the name as given in the European Inventory of Existing Commercial Chemical Substances; the classification and labelling, including whether the active substance meets any of the criteria set out in Article 5(1); physicochemical endpoints and data on pathways and environmental fate and behaviour; the result of each toxicological and ecotoxicological study; acceptable exposure level or predicted no-effect concentration established in accordance with Annex VI; the guidance on safe use provided in accordance with Annexes II and III; analytical methods referred to under Sections 5.2 and 5.3 of Title 1, and Section 4.2 of Title 2 of Annex II.

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Source: EUR-Lex (Cellar) · retrieved 2026-10-29 · Text as adopted (Official Journal); later amendments are not incorporated in this text.