3.

Notwithstanding paragraph 2, after the authorisation has been granted, access to the following information shall not in any case be refused: the name and address of the authorisation holder; the name and address of the biocidal product manufacturer; the name and address of the active substance manufacturer; the content of the active substance or substances in the biocidal product and the name of the biocidal product; physical and chemical data concerning the biocidal product; any methods for rendering the active substance or biocidal product harmless; a summary of the results of the tests required pursuant to Article 20 to establish the product’s efficacy and effects on humans, animals and the environment and, where applicable, its ability to promote resistance; recommended methods and precautions to reduce dangers from handling, transport and use as well as from fire or other hazards; safety data sheets; methods of analysis referred to in Article 19(1)(c); methods of disposal of the product and of its packaging; procedures to be followed and measures to be taken in the case of spillage or leakage; first aid and medical advice to be given in the case of injury to persons.

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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.