1. 1. An authorisation shall stipulate the terms and conditions relating to the making available on the market and use of the single biocidal product or the biocidal product family and include a summary of the biocidal product characteristics.
2. 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:
(a)((a)) trade name of the biocidal product;
(b)((b)) name and address of the authorisation holder;
(c)((c)) date of the authorisation and its date of expiry;
(d)((d)) 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;
(e)((e)) 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 %;
(f)((f)) manufacturers of the biocidal product (names and addresses including location of manufacturing sites);
(g)((g)) manufacturers of the active substances (names and addresses including location of manufacturing sites);
(h)((h)) type of formulation of the biocidal product;
(i)((i)) hazard and precautionary statements;
(j)((j)) product-type and, where relevant, an exact description of the authorised use;
(k)((k)) target harmful organisms;
(l)((l)) application doses and instructions for use;
(m)((m)) categories of users;
(n)((n)) particulars of likely direct or indirect adverse effects and first aid instructions and emergency measures to protect the environment;
(o)((o)) instructions for safe disposal of the product and its packaging;
(p)((p)) conditions of storage and shelf-life of the biocidal product under normal conditions of storage;
(q)((q)) where relevant, other information about the biocidal product.