2.

Without prejudice to Articles 66 and 67, the summary of the biocidal product characteristics for a single biocidal product or, in the case of a biocidal product family, the biocidal products within that biocidal product family, shall include the following information: trade name of the biocidal product; name and address of the authorisation holder; date of the authorisation and its date of expiry; authorisation number of the biocidal product, together with, in the case of a biocidal product family, the suffixes to apply to individual biocidal products within the biocidal product family; qualitative and quantitative composition in terms of the active substances and non-active substances, knowledge of which is essential for proper use of biocidal products; and in the case of a biocidal product family, the quantitative composition shall indicate a minimum and maximum percentage for each active and non-active substance, where the minimum percentage indicated for certain substances may be 0 %; manufacturers of the biocidal product (names and addresses including location of manufacturing sites); manufacturers of the active substances (names and addresses including location of manufacturing sites); type of formulation of the biocidal product; hazard and precautionary statements; product-type and, where relevant, an exact description of the authorised use; target harmful organisms; application doses and instructions for use; categories of users; particulars of likely direct or indirect adverse effects and first aid instructions and emergency measures to protect the environment; instructions for safe disposal of the product and its packaging; conditions of storage and shelf-life of the biocidal product under normal conditions of storage; where relevant, other information about the biocidal product.

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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.