Home Europe European Commission Commission Implementing Regulation (EU) 2023/1161 of 2 June ...
Date: 2023-06-15 Category: Not Applicable State: Union Government Country: Europe

Commission Implementing Regulation (EU) 2023/1161 of 2 June 2023 granting a Union authorisation for the single biocidal product ‘Spray On’ in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance)

Issued by European Commission · Directorate-General for Health and Food Safety

Research with AI Agent Chat with Document Generate Summary Translate Helpful Share Add to Project Create Task

Executive Summary & Key Takeaways

Executive Summary: This document is Commission Implementing Regulation (EU) 2023/1161, granting Union authorisation to Laboratorium Dr. Deppe GmbH for the biocidal product "Spray On." The authorisation, numbered EU0027669-0000, is effective from July 5, 2023, until July 31, 2032. The regulation details the product's characteristics and authorised uses, as outlined in the annex. Key Points / Main Content: * **Union Authorisation:** * Spray On receives Union authorisation (EU0027669-0000) for market availability and use. * Authorisation is valid from July 5, 2023, to July 31, 2032. * The authorisation is granted to Laboratorium Dr. Deppe GmbH. * **Product Composition and Formulation:** * Active substances: Propan-1-ol (14.925%) and Propan-2-ol (44.73%). * Formulation type: AL (Any other liquid). * **Authorised Uses:** * Use 1: Disinfection of hard, non-porous small surfaces in healthcare and pharmaceutical/cosmetic industries (Product type PT02). * Use 2: Disinfection of hard, non-porous small surfaces in healthcare and food industry settings (Product type PT04). * Application: Manual, ready-to-use liquid at room temperature. * Target organisms: Bacteria, yeasts, and enveloped viruses (Use 1); Bacteria and yeasts (Use 2). * **Hazard and Precautionary Statements:** * Hazards: Highly flammable, causes serious eye damage, may cause drowsiness or dizziness, repeated exposure may cause skin dryness or cracking. * Precautionary measures: Includes keeping away from heat/sparks, avoiding breathing vapours, using outdoors or in ventilated areas, wearing eye protection, and specific first aid measures. * **General Directions for Use:** * For professional use only. * Mandatory eye protection during handling. * Storage: Store in a dry, cool, well-ventilated area, away from direct sunlight, between 0-30°C. * Shelf life: 24 months. * Disposal: According to official regulations; do not empty into drains. * **Manufacturers of Active Substances** * Lists the names and addresses of the manufacturers and manufacturing sites for Propan-1-ol and Propan-2-ol. Impact Analysis Laboratorium Dr. Deppe GmbH: * Impact: Granted authorisation to market and sell Spray On within the Union. * Action Required: Ensure product complies with the Summary of Product Characteristics (SPC) and all specified conditions of use. Professional Users (Healthcare, Food Industry): * Impact: Authorised to use Spray On for disinfection purposes as specified. * Action Required: Follow instructions for use and risk mitigation measures outlined in the SPC, including wearing eye protection. Manufacturers of Active Substances (OQ Chemicals, BASF SE, SASOL Chemie GmbH Co. KG, Stockmeier Chemie GmbH Co. KG, Brenntag GmbH): * Impact: Their substances are approved for use in the authorised biocidal product. * Action Required: Maintain the quality and specifications of the active substances as required for biocidal product use. Regulatory Bodies/Member States: * Impact: Obligation to recognise and enforce the Union authorisation. * Action Required: Ensure compliance and monitor the market for adherence to the regulation.

Key Entities Referenced

Spray On: A single biocidal product granted Union authorisation. Regulation EU No 528/2012: Regulation of the European Parliament and of the Council concerning the making available on the market and use of biocidal products. Laboratorium Dr Deppe GmbH: The company that submitted the application for Union authorisation and the authorisation holder of Spray On. European Chemicals Agency: The Agency to which Laboratorium Dr Deppe GmbH submitted the application and that submitted an opinion to the Commission. Knieler Team Propanol Family: The related reference biocidal product family to Spray On. Propan-1-ol: An active substance contained in Spray On. Propan-2-ol: An active substance contained in Spray On. Brussels: The city where the regulation was done.
Official Source Record View Original Source →
See Full Document Text
15.6.2023 EN Official Journal of the European Union L 154/1 II (Non-legislative acts) REGULATIONS COMMISSION IMPLEMENTING REGULATION (EU) 2023/1161 of 2 June 2023 granting a Union authorisation for the single biocidal product ‘Spray On’ in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance) THE EUROPEAN COMMISSION, Having regard to the Treaty on the Functioning of the European Union, Having regard to Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012concerning the making available on the market and use of biocidal products(1), and in particular Article 44(5), first subparagraph, thereof, Whereas: (1) On 23 April 2019, Laboratorium Dr Deppe GmbH submitted to the European Chemicals Agency (‘the Agency’) an application in accordance with Article 43(1) of Regulation (EU) No 528/2012 and Article 4 of Commission Implementing Regulation (EU) No 414/2013(2) for Union authorisation of the same single biocidal product, as referred to in Article 1 of that Regulation, named ‘Spray On’, of product-types 2 and 4, as described in Annex V to Regulation (EU) No 528/2012. The application was recorded under case number BC-UR051118-16 in the Register for Biocidal Products (‘the Register’). The application also indicated the application number of the related reference biocidal product family ‘Knieler & Team Propanol Family’, recorded in the Register under case number BC-AQ050985-22. (2) The same single biocidal product ‘Spray On’ contains propan-1-ol and propan-2-ol as the active substances, which are included in the Union list of approved active substances referred to in Article 9(2) of Regulation (EU) No 528/2012 for product-types 2 and 4. (3) On 8 December 2021, the Agency submitted to the Commission an opinion(3) and the draft summary of the biocidal product characteristics (‘SPC’) of ‘Spray On’ in accordance with Article 6 of Implementing Regulation (EU) No 414/2013. (4) The opinion concludes that the proposed differences between the same single biocidal product and the related reference biocidal product are limited to information which can be the subject of an administrative change in accordance with Commission Implementing Regulation (EU) No 354/2013(4), and that based on the assessment of the related reference biocidal product family ‘Knieler & Team Propanol Family’ and subject to compliance with the draft SPC, the same single biocidal product meets the conditions laid down in Article 19(1) of Regulation (EU) No 528/2012. (1) OJ L 167, 27.6.2012, p. 1. (2) Commission Implementing Regulation (EU) No 414/2013 of 6 May 2013 specifying a procedure for the authorisation of same biocidal products in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (OJ L 125, 7.5.2013, p. 4). (3) ECHA opinion for ‘Spray On’, 8 December 2021, https://echa.europa.eu/opinions-on-union-authorisation. (4) Commission Implementing Regulation (EU) No 354/2013 of 18 April 2013 on changes of biocidal products authorised in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (OJ L 109, 19.4.2013, p. 4).L 154/2 EN Official Journal of the European Union 15.6.2023 (5) On 20 October 2022, the Agency transmitted to the Commission the draft SPC in all the official languages of the Union in accordance with Article 44(4) of Regulation (EU) No 528/2012. (6) The Commission concurs with the opinion of the Agency and considers it therefore appropriate to grant a Union authorisation for the same single biocidal product ‘Spray On’. (7) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Biocidal Products, HAS ADOPTED THIS REGULATION: Article 1 A Union authorisation with authorisation number EU-0027669-0000 is granted to Laboratorium Dr Deppe GmbH for the making available on the market and use of the same single biocidal product ‘Spray On’ in accordance with the summary of the biocidal product characteristics set out in the Annex. The Union authorisation is valid from 5 July 2023until 31 July 2032. Article 2 This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union. This Regulation shall be binding in its entirety and directly applicable in all Member States. Done at Brussels, 2 June 2023. For the Commission The President Ursula VON DER LEYEN15.6.2023 EN Official Journal of the European Union L 154/3 ANNEX Summary of product characteristics for a biocidal product Spray On Product type 2 – Disinfectants and algaecides not intended for direct application to humans or animals (Disinfectants) Product type 4 – Food and feed area (Disinfectants) Authorisation number: EU-0027669-0000 R4BP asset number: EU-0027669-0000 1. ADMINISTRATIVE INFORMATION 1.1. Trade name(s) of the product Trade name(s) Spray On Medizid Rapid Pro Medizid Rapid Optima Pro MyClean DS plus MyClean DS basic Bavicid Quick Immix Clean Pro 1.2. Authorisation holder Name and address of the authorisation Name Laboratorium Dr Deppe GmbH holder Address Hooghe Weg 35, 47906 Kempen Germany Authorisation number EU-0027669-0000 R4BP asset number EU-0027669-0000 Date of the authorisation 5.7.2023 Expiry date of the authorisation 31.7.2032 1.3. Manufacturer(s) of the product Name of manufacturer Laboratorium Dr Deppe GmbH Address of manufacturer Hooghe Weg 35, 47906 Kempen Germany Location of manufacturing sites Laboratorium Dr Deppe GmbH, Hooghe Weg 35, 47906 Kempen Germany 1.4. Manufacturer(s) of the active substance(s) Active substance Propan-1-ol Name of manufacturer OQ Chemicals GmbH (formerly Oxea GmbH) Address of manufacturer Rheinpromenade 4a, 40789 Monheim am Rhein GermanyL 154/4 EN Official Journal of the European Union 15.6.2023 Location of manufacturing sites OQ Chemicals Corperation (formerly Oxea Coperation), 2001 FM 3057 TX, 77414 Bay City United States Active substance Propan-1-ol Name of manufacturer BASF SE Address of manufacturer Carl-Bosch-Str. 38, 67056 Ludwigshafen Germany Location of manufacturing sites BASF SE, Carl-Bosch-Str. 38, 67056 Ludwigshafen Germany Active substance Propan-1-ol Name of manufacturer SASOL Chemie GmbH & Co. KG Address of manufacturer Secunda Chemical Operations, Sasol Place, 50 Katherine Street, 2090 Sandton South Africa Location of manufacturing sites Secunda Chemical Operations, PDP Kruger Street, 2302 Secunda South Africa Active substance Propan-2-ol Name of manufacturer Stockmeier Chemie GmbH & Co. KG Address of manufacturer Am Stadtholz 37, 33609 Bielefeld Germany Location of manufacturing sites INEOS Solvent Germany GmbH, Römerstrasse 733, 47443 Moers Germany Active substance Propan-2-ol Name of manufacturer Brenntag GmbH Address of manufacturer Stinnes-Platz 1, 45472 Mülheim an der Ruhr Germany Location of manufacturing sites Shell Nederland Raffinaderij B.V., 3196 KK Rotterdam-Pernis Netherlands Exxon Mobil, LA 70805 Baton Rouge United States 2. PRODUCT COMPOSITION AND FORMULATION 2.1. Qualitative and quantitative information on the composition of the product Common name IUPAC name Function CAS number EC number Content (%) Propan-1-ol Active Substance 71-23-8 200-746-9 14,925 Propan-2-ol Active Substance 67-63-0 200-661-7 44,73 2.2. Type of formulation AL – Any other liquid15.6.2023 EN Official Journal of the European Union L 154/5 3. HAZARD AND PRECAUTIONARY STATEMENTS Hazard statements Highly flammable liquid and vapour. Causes serious eye damage. May cause drowsiness or dizziness. Repeated exposure may cause skin dryness or cracking. Precautionary statements Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. – No smoking. Keep container tightly closed. Avoid breathing vapours. Use only outdoors or in a well-ventilated area. Wear eye protection. Immediately call a POISON CENTRE/doctor. IF INHALED:Remove person to fresh air and keep comfortable for breathing. IF IN EYES:Rinse cautiously with water for several minutes.Remove contact lenses, if present and easy to do. Continue rinsing. Store in a well-ventilated place.Keep cool. Store locked up. Dispose of container to an authorised waste collection point. 4. AUTHORISED USE(S) 4.1. Use description Table 1 Use # 1 – hard non-porous small surface disinfection RTU liquid Product type PT02 – Disinfectants and algaecides not intended for direct application to humans or animals (Disinfectants) Where relevant, an exact description Not relevant of the authorised use Target organism(s) (including Scientific name: other development stage) Common name: Bacteria Development stage: Scientific name: other Common name: Yeasts Development stage: Scientific name: other Common name: Enveloped viruses Development stage: Field(s) of use Indoor Healthcare facilities and pharmaceutical and cosmetic industry, for example in patient-near surrounding, working areas/desks, general equipment (excluding food contact surfaces): disinfection of small hard/non-porous surfaces. For professional use only.L 154/6 EN Official Journal of the European Union 15.6.2023 Application method(s) Method: Manual application Detailed description: Ready-to-use surface disinfectant at room temperature (20 ± 2 °C). The entire surface to be disinfected is wetted by pouring or spraying from short distance and subsequently thoroughly wiped with a cloth. The amount of product should be sufficient (max. 50 ml/m2) to keep the surface wet during the contact time. Application rate(s) and frequency Application Rate: Minimum exposure time: • for the control of bacteria, yeasts and enveloped viruses: 60 sec Dilution (%): Ready-to-use product Number and timing of application: A reasonable frequency of disinfection in a patient’s room is 1–2 per day. Maximum number of applications is 6 per day. No safety intervals need to be considered between the application phases. Category(ies) of users Industrial Professional Pack sizes and packaging material 125, 150, 500, 1 000ml transparent/white high-density polyethylene (HDPE) bottle with polypropylene (PP) flip top caps (accessory: PP screw closure with spray head); 5 000ml transparent/white HDPE canister with HDPE screwed cap. 4.1.1. Use-specific instructions for use Surfaces should always be visibly clean prior to disinfection. Maximum number of applications is 6 per day. 4.1.2. Use-specific risk mitigation measures See general directions for use. 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 See general directions for use. 4.1.4. Where specific to the use, the instructions for safe disposal of the product and its packaging See general directions for use. 4.1.5. Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage See general directions for use. 4.2. Use description Table 2 Use # 2 – hard non-porous small surface disinfection RTU liquid Product type PT04 – Food and feed area (Disinfectants) Where relevant, an exact description Not relevant of the authorised use15.6.2023 EN Official Journal of the European Union L 154/7 Target organism(s) (including Scientific name: other development stage) Common name: Bacteria Development stage: Scientific name: other Common name: Yeasts Development stage: Field(s) of use Indoor Healthcare facilities and in food industry, for example food preparation and handling in kitchens/restaurants): disinfection of small hard/non-porous surfaces. For professional use only. Application method(s) Method: Manual application Detailed description: Ready-to-use surface disinfectant at room temperature (20 ± 2 °C). The entire surface to be disinfected is wetted by pouring or spraying from short distance and subsequently thoroughly wiped with a cloth. The amount of product should be sufficient (max. 50 ml/m2) to keep the surface wet during the contact time. Application rate(s) and frequency Application rate: Minimum exposure time: for the control of bacteria and yeasts at 20 °C: 60 sec Dilution (%): Ready-to-use product Number and timing of application: The products can be used as often as necessary. A reasonable frequency in kitchens is 1–2 per day. No safety intervals need to be considered between the application phases. Category(ies) of users Industrial Professional Pack sizes and packaging material 125, 150, 500, 1 000ml transparent/white high-density polyethylene (HDPE) bottle with polypropylene (PP) flip top caps (accessory: PP screw closure with spray head); 5 000ml transparent/white HDPE canister with HDPE screwed cap. 4.2.1. Use-specific instructions for use Surfaces should always be visibly clean prior to disinfection. 4.2.2. Use-specific risk mitigation measures See general directions for use. 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 See general directions for use. 4.2.4. Where specific to the use, the instructions for safe disposal of the product and its packaging See general directions for use.L 154/8 EN Official Journal of the European Union 15.6.2023 4.2.5. Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage See general directions for use. 5. GENERAL DIRECTIONS FOR USE(1) 5.1. Instructions for use For professional use only. 5.2. Risk mitigation measures The use of eye protection during handling of the product is mandatory. Keep out of reach of children. 5.3. Particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment First-aid measures general: Move the affected person away from the contaminated area. Get medical advice/attention if you feel unwell. If possible show this sheet. IF INHALED: Move to fresh air and keep at rest in a position comfortable for breathing. Call a POISON CENTRE or a doctor. IF ON SKIN: Immediately wash skin with plenty of water. Thereafter take off all contaminated clothing and wash it before reuse. Continue to wash the skin with water for 15 minutes. Call a POISON CENTRE or a doctor. IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing for at least 15 minutes. Call 112/ambulance for medical assistance. Information to Healthcare personnel/doctor: The eyes should also be rinsed repeatedly on the way to the doctor if eye exposure to alkaline chemicals (pH > 11), amines and acids like acetic acid, formic acid or propionic acid. IF SWALLOWED: Immediately rinse mouth. Give something to drink, if exposed person is able to swallow. Do NOT induce vomiting. Call 112/ambulance for medical assistance. Accidental release measures: Stop leak if safe to do so. Remove ignition sources. Use special care to avoid static electric charges. No open flames. No smoking. Prevent entry to sewers and public waters. Wipe up with absorbent material (for example cloth). Soak up spills with inert solids, such as clay or diatomaceous earth as soon as possible. Take up mechanically (sweeping, shovelling). Dispose of in accordance with relevant local regulations. 5.4. Instructions for safe disposal of the product and its packaging Disposal must be done according to official regulations. Do not empty into drains. Do not dispose of with domestic waste. Dispose of contents/container to an authorised waste collection point. Empty the packaging completely prior to disposal. When totally empty, containers are recyclable like any other packing. 5.5. Conditions of storage and shelf-life of the product under normal conditions of storage Shelf-life: 24 months Store in dry, cool, well-ventilated area. Keep container tightly closed. Keep out of direct sunlight. Recommended storage temperature: 0–30 °C (1) Instructions for use, risk mitigation measures and other directions for use under this section are valid for any authorised uses.15.6.2023 EN Official Journal of the European Union L 154/9 Do not store at temperatures below 0 °C Do not store near food, drink and animal feedingstuff. Keep away from combustible material. 6. OTHER INFORMATION

Continue your research