Commission Implementing Regulation (EU) 2025/2200of 21 October 2025amending Implementing Regulation (EU) 2022/1186 as regards administrative changes to the Union authorisation of the biocidal product family L+R Propanol PT1 Family(Text with EEA relevance)
European Union
Commission Implementing Regulation (EU) 2025/2200 of 21 October 2025 amending Implementing Regulation (EU) 2022/1186 as regards administrative changes to the Union authorisation of the biocidal product family L+R Propanol PT1 Family (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 2012 concerning the making available on the market and use of biocidal products OJ L 167, 27.6.2012, p. 1, ELI: http://data.europa.eu/eli/reg/2012/528/oj. , and in particular Article 50(2) thereof, Whereas: (1) On 8 July 2022, Commission Implementing Regulation (EU) 2022/1186 Commission Implementing Regulation (EU) 2022/1186 of 8 July 2022 granting a Union authorisation for the biocidal product family L+R Propanol PT1 Family (OJ L 184, 11.7.2022, p. 41, ELI: http://data.europa.eu/eli/reg_impl/2022/1186/oj). granted a Union authorisation with authorisation number EU-0027466-0000, to Lohmann & Rauscher International GmbH&Co.KG for the making available on the market and use of the biocidal product family L+R Propanol PT1 Family. The Annex to that Implementing Regulation provides the summary of product characteristics for that biocidal product family. (2) On 2 June 2025, Lohmann & Rauscher International GmbH&Co.KG submitted to the European Chemicals Agency (the Agency) a notification in accordance with Article 11(1) of Commission Implementing Regulation (EU) No 354/2013 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, ELI: http://data.europa.eu/eli/reg_impl/2013/354/oj). of administrative changes to the Union authorisation for the biocidal product family L+R Propanol PT1 Family, as referred to in Title 1, Sections 1 and 2, of the Annex to that Implementing Regulation. The notification was recorded in the Register for Biocidal Products under case number BC-XW106193-09. (3) The notified proposed changes to the authorisation concern the transfer of the authorisation to a new holder established in the European Economic Area, a change in the family name and product names, the addition and deletion of trade names, the addition and deletion of product manufacturers and the addition of new active substance manufacturers. (4) On 30 June 2025, the Agency submitted to the Commission, in accordance with Article 11(3) of Implementing Regulation (EU) No 354/2013, an opinion ECHA Opinion No UTR-C_1835532-78-00/F of 30 June 2025 on the administrative change of the Union authorisation of the biocidal product family L+R Propanol PT1 Family, https://echa.europa.eu/opinions-on-union-authorisation. on the notified administrative changes to the Union authorisation for the biocidal product family L+R Propanol PT1 Family, together with a revised summary of the biocidal product characteristics. In the opinion, the Agency concludes that the proposed changes are administrative changes as referred to in Article 50(3), point (a), of Regulation (EU) No 528/2012 and as specified in Title 1, Sections 1 and 2, of the Annex to Implementing Regulation (EU) No 354/2013, and that after the implementation of the changes, the conditions of Article 19 of Regulation (EU) No 528/2012 will still be met.
(5) On 30 June 2025, the Agency transmitted to the Commission the revised summary of the biocidal product characteristics of the Union authorisation for the biocidal product family L+R Propanol PT1 Family in all official languages of the Union, covering all the administrative changes applied for, in accordance with Article 11(6) of Implementing Regulation (EU) No 354/2013. (6) The Commission concurs with the opinion of the Agency and therefore considers it appropriate to amend the Union authorisation for the biocidal product family L+R Propanol PT1 Family to transfer the authorisation to Schuelke & Mayr GmbH and to introduce the other administrative changes requested. (7) Except for the amendments regarding the administrative changes, all other information included in the summary of the biocidal product characteristics of L+R Propanol PT1 Family as set out in Annex to Implementing Regulation (EU) 2022/1186 remains unchanged. (8) In order to enhance clarity and to ease the access of users and interested parties to the consolidated version of the summary of the biocidal product characteristics which is to be published by the Agency, the Annex to Implementing Regulation (EU) 2022/1186 should be replaced in its entirety. Due to a change in the format used for the generation of the summary of biocidal product characteristics in the Register for Biocidal Products in February 2024, the summary of biocidal product characteristics in that Annex should also include some minor editorial and layout changes. (9) Implementing Regulation (EU) 2022/1186 should therefore be amended accordingly, HAS ADOPTED THIS REGULATION:
Article 1
The Annex to Implementing Regulation (EU) 2022/1186 is replaced by the text in the Annex to this Regulation.
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, 21 October 2025. For the Commission The President Ursula von der Leyen
Annex
ANNEX SUMMARY OF PRODUCT CHARACTERISTICS FOR A BIOCIDAL PRODUCT FAMILY Propanol PT1 Family Product type(s) PT01: Human hygiene Authorisation number: EU-0027466-00 R4BP asset number: EU-0027466-0000 PART I FIRST INFORMATION LEVEL
- ADMINISTRATIVE INFORMATION 1.1. Family name NamePropanol PT1 Family 1.2. Product type(s) Product type(s)PT01: Human hygiene 1.3. Authorisation holder 1.4. Manufacturer(s) of the product Name and address of the authorisation holderNameSchülke & Mayr GmbHAddressRobert-Koch-Str. 2 22851 Norderstedt GermanyAuthorisation numberEU-0027466-00R4BP asset numberEU-0027466-0000Date of the authorisation31.7.2022Expiry date of the authorisation30.6.2032Name of manufacturerSchülke & Mayr GmbHAddress of manufacturerRobert-Koch-Str. 2 22851 Norderstedt GermanyLocation of manufacturing sitesSchülke & Mayr GmbH site 1 Robert-Koch-Str. 2 22851 Norderstedt GermanyName of manufacturerA.F.P. Antiseptica Forschungs- und Produktionsgesellschaft mbHAddress of manufacturerOtto-Brenner-Straße 16 21337 Lüneburg Germany
Location of manufacturing sitesA.F.P. Antiseptica Forschungs- und Produktionsgesellschaft mbH site 1 Otto-Brenner-Straße 16 21337 Lüneburg Germany 1.5. Manufacturer(s) of the active substance(s) Active substancePropan-2-olName of manufacturerINEOS Solvent Germany GmbHAddress of manufacturerRömerstrasse 733 47443 Moers GermanyLocation of manufacturing sitesINEOS Solvent Germany GmbH site 1 INEOS Solvent Germany GmbH, Römerstrasse 733 47443 Moers GermanyActive substancePropan-2-olName of manufacturerIneos Solvents Germany GmbH (formerly Sasol)Address of manufacturerRömerstraße 733 47443 Moers GermanyLocation of manufacturing sitesIneos Solvents Germany GmbH (formerly Sasol) site 2 Shamrockstr. 88 44623 Herne GermanyActive substancePropan-2-olName of manufacturerShell Chemicals Europe B.V.Address of manufacturerPostbus 2334 3000 CH Rotterdam Netherlands (the)Location of manufacturing sitesShell Chemicals Europe B.V. site 1 BV/Shell Nederland Raffinaderij B.V. Vondelingenweg 601 3196 KK Rotterdam-Pernis Netherlands (the)Active substancePropan-1-olName of manufacturerOQ Chemicals GmbH (formerly OXEA)Address of manufacturerRheinpromenade 4a 40789 Monheim am Rhein GermanyLocation of manufacturing sitesOQ Chemicals GmbH (formerly OXEA) site 1 OQ Chemicals Corporation, 2001 FM 3057 (formerly OXEA Corporation) TX 77414-2968 Bay City United States (the)Active substancePropan-1-olName of manufacturerSasol Chemie GmbH & Co. KG Address of manufacturerSecunda Chemical Operations, Sasol Place, 50 Katherine Street 2090 Sandton South AfricaLocation of manufacturing sitesSasol Chemie GmbH & Co. KG site 1 Secunda Chemical Operations, PDP Kruger Street 2302 Secunda South AfricaActive substancePropan-1-olName of manufacturerBASF SEAddress of manufacturerCarl-Bosch-Str. 38 67056 Ludwigshafen GermanyLocation of manufacturing sitesBASF SE site 1 BASF SE, Carl-Bosch-Str. 38 67056 Ludwigshafen Germany 2. PRODUCT FAMILY COMPOSITION AND FORMULATION 2.1. Qualitative and quantitative information on the composition of the family Common nameIUPAC nameFunctionCAS numberEC numberContent (%)Propan-2-olActive substance67-63-0200-661-745 - 45 % (w/w)Propan-1-olActive substance71-23-8200-746-930 - 30 % (w/w)TetradecanolMyristil alcoholNon-active substance112-72-1204-000-30 - 0,95 % (w/w) 2.2. Type(s) of formulation Formulation type(s)AL Any other liquid PART II SECOND INFORMATION LEVEL META SPC(S)
- META SPC 1 ADMINISTRATIVE INFORMATION 1.1. Meta SPC 1 identifier IdentifierMeta SPC: meta SPC 1 1.2. Suffix to the authorisation number Number1-1 1.3. Product type(s) Product type(s)PT01: Human hygiene
- META SPC 1 COMPOSITION 2.1. Qualitative and quantitative information on the composition of the meta SPC 1 Common nameIUPAC nameFunctionCAS numberEC numberContent (%)Propan-2-olActive substance67-63-0200-661-745 - 45 % (w/w)Propan-1-olActive substance71-23-8200-746-930 - 30 % (w/w)TetradecanolMyristil alcoholNon-active substance112-72-1204-000-30,95 - 0,95 % (w/w) 2.2. Type(s) of formulation of the meta SPC 1
Formulation type(s)AL Any other liquid 3. HAZARD AND PRECAUTIONARY STATEMENTS OF THE META SPC 1 Hazard statements H226: Flammable liquid and vapour. H318: Causes serious eye damage. H412: Harmful to aquatic life with long lasting effects. H336: May cause drowsiness or dizziness. EUH066: Repeated exposure may cause skin dryness or cracking. Precautionary statements P210: Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. P233: Keep container tightly closed. P261: Avoid breathing vapours. P271: Use only outdoors or in a well-ventilated area. P273: Avoid release to the environment. P304+P340: IF INHALED: Remove person to fresh air and keep comfortable for breathing. P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P310: Immediately call a POISON CENTER / doctor. P403+P235: Store in a well-ventilated place. Keep cool. P405: Store locked up. P501: Dispose of container to an approved waste disposal plant. 4. AUTHORISED USE(S) OF THE META SPC 4.1. Use description Table 1 Hygienic handrub Product typePT01: Human hygieneWhere relevant, an exact description of the authorised useNot relevant.Target organism(s) (including development stage) Scientific name: other Common name: Bacteria Development stage: no data Scientific name: other Common name: Yeasts Development stage: no data Scientific name: other Common name: Mycobacteria Development stage: no data Scientific name: other Common name: viruses (limited spectrum of virucidal activity) Development stage: no data Field(s) of use indoor use hospitals and other health care institutions, ambulances, surgeries, nursing homes (including home-care of patients), hospital canteens, large kitchens, pharmaceutical industries, production sites, laboratories: hygienic handrub onto visibly clean and dry hands. for professional use only. Application method(s) Method: manual application Detailed description: Rubbing Application rate(s) and frequency Application Rate: Dosage: At least 3 ml (use dispensers: for example set to 1,5 ml per stroke, 2 strokes per 3 ml). Minimum contact time: 30 sec ready-to-use product Number and timing of application: There is no restriction in the number and timing of applications. No safety intervals need to be considered between the application phases. The product may be used at any time and as often as required. Category(ies) of users industrial professional Pack sizes and packaging material100 ml, 500 ml and 1000 ml in transparent HDPE bottles with PP flip top cap. 4.1.1. Use-specific instructions for use The products can be applied directly, or the products can be used in a dispenser or with a pump. For hygienic handrub use 3 ml of product and keep hands wet for 30 seconds. 4.1.2. Use-specific risk mitigation measures See general directions for use of meta SPC 1 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 of meta SPC 1 4.1.4. Where specific to the use, the instructions for safe disposal of the product and its packaging See general directions for use of meta SPC 1 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 of meta SPC 1 4.2. Use description Table 2 Surgical handrub Product typePT01: Human hygieneWhere relevant, an exact description of the authorised useNot relevant.Target organism(s) (including development stage) Scientific name: other Common name: Bacteria Development stage: no data Scientific name: other Common name: Yeasts Development stage: no data Scientific name: other Common name: Mycobacteria Development stage: no data Scientific name: other Common name: viruses (limited spectrum of virucidal activity) Development stage: no data Field(s) of use indoor use hospitals and other health care institutions: surgical handrub onto visibly clean and dry hands and forearms. For professional use only. Application method(s) Method: manual application Detailed description: Rubbing Application rate(s) and frequency Application Rate: Dosage: in portions of 3 ml (use dispensers: for example set to 1,5 ml per stroke, 2 strokes per 3 ml). Minimum exposure time: 90s ready-to-use product Number and timing of application: There is no restriction in the number and timing of applications. No safety intervals need to be considered between the application phases. The product may be used at any time and as often as required. Category(ies) of usersprofessionalPack sizes and packaging material100 ml, 500 ml and 1000 ml in transparent HDPE bottles with PP flip top cap. 4.2.1. Use-specific instructions for use The products can be applied directly or the products can be used in a dispenser or with a pump. For surgical handrub use as many portions of 3 ml as necessary to keep hands wet for 90 seconds. 4.2.2. Use-specific risk mitigation measures See general directions for use of meta SPC 1 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 of meta SPC 1 4.2.4. Where specific to the use, the instructions for safe disposal of the product and its packaging See general directions for use of meta SPC 1 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 of meta SPC 1 5. GENERAL DIRECTIONS FOR USE OF THE META SPC 1 5.1. Instructions for use For professional use only. 5.2. Risk mitigation measures Avoid contact with eyes. 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 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 INHALED: Move to fresh air and keep at rest in a position comfortable for breathing. 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. After spilling: Take up with absorbent material (for example sand, kieselgur, universal binder). When picked up, treat material as prescribed under Disposal considerations. 5.4. Instructions for safe disposal of the product and its packaging Residuals must be removed from packaging and when emptied completely disposed of in accordance with the regulations for waste removal. Incompletely emptied packaging must be disposed of in the form of disposal specified by the regional disposer. 5.5. Conditions of storage and shelf-life of the product under normal conditions of storage Technical measures and storage conditions: Shelf-life: 36 months Keep container tightly closed and dry in a cool, well-ventilated place. Protect from direct sunlight. Recommended storage temperature: 0-30°C Requirements for storage rooms and vessels: Containers which are opened must be carefully closed and kept upright to prevent leakage. Always keep in containers of same material as the original one. Advice on storage assembly: Do not store together with: oxidizing substances; spontaneously combusting substances. 6. OTHER INFORMATION 7. THIRD INFORMATION LEVEL: INDIVIDUAL PRODUCTS IN THE META SPC 1 7.1. Trade name(s), authorisation number and specific composition of each individual product Trade name(s)desmanol protectMarket area: EUdesmanol plusMarket area: EUdesmanol proMarket area: EUdesmanol ultraMarket area: EUdesmanol clinpureMarket area: EUdesmanol advancedMarket area: EUdesmanol ethanolfreeMarket area: EUdesmanol pro pureMarket area: EUsensiva protectMarket area: EUvirusept protectMarket area: EU septodermMarket area: EUmicroshieldMarket area: EUHalasept 710Market area: EUAuthorisation numberEU-0027466-0001 1-1Common nameIUPAC nameFunctionCAS numberEC numberContent (%)Propan-2-olActive substance67-63-0200-661-745 % (w/w)Propan-1-olActive substance71-23-8200-746-930 % (w/w)TetradecanolMyristil alcoholNon-active substance112-72-1204-000-30,95 % (w/w)
- META SPC 2 ADMINISTRATIVE INFORMATION 1.1. Meta SPC 2 identifier IdentifierMeta SPC: meta SPC 2 1.2. Suffix to the authorisation number Number1-2 1.3. Product type(s) Product type(s)PT01: Human hygiene
- META SPC 2 COMPOSITION 2.1. Qualitative and quantitative information on the composition of the meta SPC 2 Common nameIUPAC nameFunctionCAS numberEC numberContent (%)Propan-2-olActive substance67-63-0200-661-745 - 45 % (w/w)Propan-1-olActive substance71-23-8200-746-930 - 30 % (w/w)
2.2. Type(s) of formulation of the meta SPC 2 Formulation type(s)AL Any other liquid 3. HAZARD AND PRECAUTIONARY STATEMENTS OF THE META SPC 2 Hazard statements H226: Flammable liquid and vapour. H318: Causes serious eye damage. H336: May cause drowsiness or dizziness. EUH066: Repeated exposure may cause skin dryness or cracking. Precautionary statements P210: Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. P233: Keep container tightly closed. P261: Avoid breathing vapours. P271: Use only outdoors or in a well-ventilated area. P304+P340: IF INHALED: Remove person to fresh air and keep comfortable for breathing. P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P310: Immediately call a POISON CENTER/doctor. P403+P235: Store in a well-ventilated place. Keep cool. P405: Store locked up. P501: Dispose of container to an approved waste disposal plant. 4. AUTHORISED USE(S) OF THE META SPC 4.1. Use description Table 1 Hygienic handrub Product typePT01: Human hygieneWhere relevant, an exact description of the authorised useNot relevantTarget organism(s) (including development stage) Scientific name: other Common name: Bacteria Development stage: no data Scientific name: other Common name: Yeasts Development stage: no data Scientific name: other Common name: Mycobacteria Development stage: no data Scientific name: other Common name: viruses (limited spectrum of virucidal activity) Development stage: no data Field(s) of use indoor use hospitals and other health care institutions, ambulances, surgeries, nursing homes (including home-care of patients), hospital canteens, large kitchens, pharmaceutical industries, production sites, laboratories: hygienic handrub onto visibly clean and dry hands. for professional use only. Application method(s) Method: manual application Detailed description: Rubbing Application rate(s) and frequency Application Rate: Dosage: At least 3 ml (use dispensers: for example set to 1,5 ml per stroke, 2 strokes per= 3 ml). Minimum exposure time: 30s ready-to-use product Number and timing of application: There is no restriction in the number and timing of applications. No safety intervals need to be considered between the application phases. The product may be used at any time and as often as required. Category(ies) of users industrial professional Pack sizes and packaging material100 ml, 500 ml and 1000 ml in transparent HDPE bottles with PP flip top cap. 4.1.1. Use-specific instructions for use The products can be applied directly or the products can be used with a dispenser or with a pump. For hygienic handrub use 3 ml of product and keep hands wet for 30 seconds. 4.1.2. Use-specific risk mitigation measures See general directions for use of meta SPC 2 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 of meta SPC 2 4.1.4. Where specific to the use, the instructions for safe disposal of the product and its packaging See general directions for use of meta SPC 2 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 of meta SPC 2 4.2. Use description Table 2 Surgical handrub Product typePT01: Human hygieneWhere relevant, an exact description of the authorised useNot relevant.Target organism(s) (including development stage) Scientific name: other Common name: Bacteria Development stage: no data Scientific name: other Common name: Yeasts Development stage: no data Scientific name: other Common name: Mycobacteria Development stage: no data Scientific name: other Common name: viruses (limited spectrum of virucidal activity) Development stage: no data Field(s) of use indoor use Hospitals and other health care institutions: surgical handrub onto visibly clean and dry hands and forearms. For professional use only. Application method(s) Method: manual application Detailed description: Rubbing Application rate(s) and frequency Application Rate: Dosage: in portions of 3 ml (use dispensers: for example set to 1,5 ml per stroke, 2 strokes per 3 ml). Minimum exposure time: 90s ready-to-use product Number and timing of application: There is no restriction in the number and timing of applications. No safety intervals need to be considered between the application phases. The product may be used at any time and as often as required. Category(ies) of usersprofessionalPack sizes and packaging material100 ml, 500 ml and 1000 ml in transparent HDPE bottles with PP flip top cap. 4.2.1. Use-specific instructions for use The products can be applied directly or the products can be used with a dispenser or with a pump. For surgical handrub use as many portions of 3 ml as necessary to keep hands wet for 90 seconds. 4.2.2. Use-specific risk mitigation measures See general directions for use of meta SPC 2. 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 of meta SPC 2. 4.2.4. Where specific to the use, the instructions for safe disposal of the product and its packaging See general directions for use of meta SPC 2. 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 of meta SPC 2. 5. GENERAL DIRECTIONS FOR USE OF THE META SPC 2 5.1. Instructions for use For professional use only 5.2. Risk mitigation measures Avoid contact with eyes. 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 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 INHALED: Move to fresh air and keep at rest in a position comfortable for breathing. 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. After spilling: Take up with absorbent material (for example sand, kieselgur, universal binder). When picked up, treat material as prescribed under Disposal considerations. 5.4. Instructions for safe disposal of the product and its packaging Residuals must be removed from packaging and when emptied completely disposed of in accordance with the regulations for waste removal. Incompletely emptied packaging must be disposed of in the form of disposal specified by the regional disposer. 5.5. Conditions of storage and shelf-life of the product under normal conditions of storage Technical measures and storage conditions: Shelf-life: 36 months Keep container tightly closed and dry in a cool, well-ventilated place. Protect from direct sunlight. Recommended storage temperature: 0-30°C Requirements for storage rooms and vessels: Containers which are opened must be carefully closed and kept upright to prevent leakage. Always keep in containers of same material as the original one. Advice on storage assembly: Do not store together with: oxidizing substances; spontaneously combusting substances 6. OTHER INFORMATION 7. THIRD INFORMATION LEVEL: INDIVIDUAL PRODUCTS IN THE META SPC 2 7.1. Trade name(s), authorisation number and specific composition of each individual product Trade name(s)desmanol pure protectMarket area: EUdesmanol pure+Market area: EU desmanol pure proMarket area: EUdesmanol pure guardMarket area: EUdesmanol expertMarket area: EUdesmanol pure ultraMarket area: EUdesmanol EFMarket area: EUdesmanol clearMarket area: EUsensiva pureMarket area: EUvirusept pureMarket area: EUseptoderm pureMarket area: EUmicroshield pureMarket area: EUHalasept 720Market area: EUAuthorisation numberEU-0027466-0002 1-2Common nameIUPAC nameFunctionCAS numberEC numberContent (%)Propan-2-olActive substance67-63-0200-661-745 % (w/w)Propan-1-olActive substance71-23-8200-746-930 % (w/w) 7.2. Trade name(s), authorisation number and specific composition of each individual product Trade name(s)desmanol pure universalMarket area: EUdesmanol pure plusMarket area: EUdesmanol pure expertMarket area: EU desmanol proshieldMarket area: EUdesmanol healthcareMarket area: EUdesmanol duoMarket area: EUdesmanol EtOH-freeMarket area: EUdesmanol zeroMarket area: EUsensiva pure+Market area: EUvirusept expertMarket area: EUseptoderm pure+Market area: EUmicroshield pure+Market area: EUHalasept 740Market area: EUAuthorisation numberEU-0027466-0003 1-2Common nameIUPAC nameFunctionCAS numberEC numberContent (%)Propan-2-olActive substance67-63-0200-661-745 % (w/w)Propan-1-olActive substance71-23-8200-746-930 % (w/w)
Metadata
- Type
- Forordning
- År
- 2025
- Ikrafttrædelsesdato
- 1. januar 1970