Commission Implementing Regulation (EU) 2024/1674 of 13 June 2024 granting a Union authorisation for the single biocidal product SANICALCO Q in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council

Table of Contents

• Commission Implementing Regulation (EU) 2024/1674 of 13 June 2024 granting a Union authorisation for the single biocidal product SANICALCO Q in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council 1
• ANNEX SUMMARY OF PRODUCT CHARACTERISTICS FOR A BIOCIDAL PRODUCT 3
• 1.ADMINISTRATIVE INFORMATION 3
• 1.1.Trade name(s) of the product 3
• 1.2.Authorisation holder 3
• 1.3.Manufacturer(s) of the product 3
• 1.4.Manufacturer(s) of the active substance(s) 4
• 2.PRODUCT COMPOSITION AND FORMULATION 5
• 2.1.Qualitative and quantitative information on the composition of the product 5
• 2.2.Type(s) of formulation 6
• 3.HAZARD AND PRECAUTIONARY STATEMENTS 6
• 4.AUTHORISED USE(S) 6
• 4.1.Use description 6
• 4.1.1.Use-specific instructions 7
• 4.1.2.Use-specific risk mitigation measures 7
• 4.1.3.Where specific to the use, the particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment 8
• 4.1.4.Where specific to the use, the instructions for safe disposal of the product and its packaging 8
• 4.1.5.Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage 8
• 4.2.Use description 8
• 4.2.1.Use-specific instructions 9
• 4.2.2.Use-specific risk mitigation measures 9
• 4.2.3.Where specific to the use, the particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment 10
• 4.2.4.Where specific to the use, the instructions for safe disposal of the product and its packaging 10
• 4.2.5.Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage 10
• 4.3.Use description 10
• 4.3.1.Use-specific instructions 11
• 4.3.2.Use-specific risk mitigation measures 11
• 4.3.3.Where specific to the use, the particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment 12
• 4.3.4.Where specific to the use, the instructions for safe disposal of the product and its packaging 12
• 4.3.5.Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage 12
• 4.4.Use description 12
• 4.4.1.Use-specific instructions 13
• 4.4.2.Use-specific risk mitigation measures 13
• 4.4.3.Where specific to the use, the particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment 13
• 4.4.4.Where specific to the use, the instructions for safe disposal of the product and its packaging 14
• 4.4.5.Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage 14
• 5.GENERAL DIRECTIONS FOR USE 14
• 5.1.Instructions for use 14
• 5.2.Risk mitigation measures 14
• 5.3.Particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment 14
• 5.4.Instructions for safe disposal of the product and its packaging 14
• 5.5.Conditions of storage and shelf-life of the product under normal conditions of storage 14
• 6.OTHER INFORMATION 15