Commission Implementing Regulation (EU) 2024/2188 of 3 September 2024 granting a Union authorisation for the biocidal product family Kersia’s Lactic acid based products in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance)
Grade B
mapped from publisher markup. A grade says how a document's structure was obtained, not how reliable the law is.
Address https://gelex.eu/eli/EU/regulation/2024/2188@2024-09-03/en
Contents
- Preamble
- ANNEX
- ANNEX SUMMARY OF PRODUCT CHARACTERISTICS FOR A BIOCIDAL PRODUCT FAMILY
- Kersia’s Lactic acid based products
- PART I FIRST INFORMATION LEVEL
- 1.
- 2.
- PART II SECOND INFORMATION LEVEL - META SPC(S)
- 1.
- 2.
- 4.
- 4.1. Table 1 Disinfection of teats of milk producing animals by manual or automated dipping, foaming or spraying after milking
- 5.
- 7.
- 4.1. Table 1 Disinfection of teats of milk producing animals by manual or automated dipping after milking
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, and in particular Article 44(5), first subparagraph, thereof,
Whereas:
(1) On 26 April 2019, HYPRED SAS submitted to the European Chemicals Agency (the Agency) an application in accordance with Article 43(1) of Regulation (EU) No 528/2012 for a Union authorisation of a biocidal product family named Kersia’s Lactic acid based products of product-type 3, as described in Annex V to that Regulation, providing written confirmation that the competent authority of the Netherlands had agreed to evaluate the application. The application was recorded under case number BC-CH051281-59 in the Register for Biocidal Products.
(2) Kersia’s Lactic acid based products contains L-(+)-lactic acid as the active substance, included in the Union list of approved active substances referred to in Article 9(2) of Regulation (EU) No 528/2012 for product-type 3.
(3) On 30 November 2022, the evaluating competent authority submitted, in accordance with Article 44(1) of Regulation (EU) No 528/2012, an assessment report and the conclusions of its evaluation to the Agency.
(4) On 30 June 2023, the Agency submitted to the Commission its opinion, the draft summary of the biocidal product characteristics (SPC) of Kersia’s Lactic acid based products and the final assessment report on the biocidal product family, in accordance with Article 44(3) of Regulation (EU) No 528/2012.
(5) The opinion concludes that Kersia’s Lactic acid based products is a biocidal product family within the meaning of Article 3(1), point (s), of Regulation (EU) No 528/2012, that it is eligible for Union authorisation in accordance with Article 42(1) of that Regulation and that, subject to compliance with the draft SPC, it meets the conditions laid down in Article 19(1) and (6) of that Regulation. The opinion does not recommend the authorisation of the use of the products as teat disinfectants applied prior to milking, due to an exceedance of the acceptable daily intake of a co-formulant contained in all products of the biocidal product family Kersia’s Lactic acid based products.
(6) On 13 July 2023, 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.
(7) The Commission concurs with the opinion of the Agency and considers it therefore appropriate to grant a Union authorisation for the biocidal product family Kersia’s Lactic acid based products in accordance with the recommendations in that opinion.
(8) 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-0031195-0000 is hereby granted to HYPRED SAS for the making available on the market and use of the biocidal product family Kersia’s Lactic acid based products subject to compliance with the summary of the biocidal product characteristics set out in the Annex. The Union authorisation is valid from 24 September 2024 to 31 August 2034.
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, 3 September 2024. For the Commission The President Ursula von der Leyen
ANNEX
ANNEX SUMMARY OF PRODUCT CHARACTERISTICS FOR A BIOCIDAL PRODUCT FAMILY
Kersia’s Lactic acid based products
Product type(s) PT03: Veterinary hygiene Authorisation number EU-0031195-0000 R4BP asset number EU-0031195-0000
PART I FIRST INFORMATION LEVEL
1. ADMINISTRATIVE INFORMATION
1.
1.1. Family name Name Kersia’s Lactic acid based products
1.2. Product type(s) Product type(s) PT03: Veterinary hygiene
1.3. Authorisation holder Name and address of the authorisation holder Name HYPRED SAS Address 55, boulevard Jules Verger 35803 DINARD FR Authorisation number EU-0031195-0000 R4BP asset number EU-0031195-0000 Date of the authorisation 24 September 2024 Expiry date of the authorisation 31 August 2034
1.4. Manufacturer(s) of the product Name of manufacturer HYPRED SAS - KERSIA Group Address of manufacturer 55, Boulevard Jules Verger BP10180 35803 DINARD France Location of manufacturing sites HYPRED SAS - KERSIA Group 55, Boulevard Jules Verger; BP 10180 35803 DINARD Cedex France HYPRED SAS - KERSIA Group Zone Industrielle Le Roineau 72500 VAAS France Medentech Ltd – KERSIA Group Clonard Road Y35Y7WY WEXFORD Ireland SOPURA – KERSIA Group Parc Paysager de Tyberchamps 14 7180 SENEFFE Belgium KERSIA DEUTSCHLAND GmbH Marie-Curie-Straße 23 53332 BORNHEIM – SECHTEM Germany Holchem Laboratories Ltd – KERSIA Group Gateway House, Pilsworth Road, Pilsworth Industrial Estate BL9 8RD Bury United Kingdom of Great Britain and Northern Ireland (the) KERSIA AUSTRIA GmbH PFONGAUERSTRAßE 17 5202 NEUMARKT AM WALLERSEE Austria KERSIA POLSKA Sp.z.o.o Niepruszewo, ul. Kasztanowa 4 64-320 BUK Poland KERSIA ITALIA S.r.l Strada Montodine – Gombito; Loc. Cà Nova 26010 RIPALTA ARPINA (CR) Italy KERSIA IBERICA SL Pol. Miguel Eguía C/Zarapuz s/n 31200 ESTELLA (NAVARRA) Spain Kilco Holdings Ltd – KERSIA Group Broomhouses 2 Industrial Estate; Old Glasgow Road DG11 2SD LOCKERBIE United Kingdom of Great Britain and Northern Ireland (the) Kilco (International) Ltd – KERSIA Group 1A Trench Road Mallusk; Newtownabbey BT36 4TY CO ANTRIM Ireland SOPURA Quimica – KERSIA Group Pol. Ind. La Canaleta; Avinguda Júpiter n° 7 25300 TARREGA (LLEIDA) Spain KERSIA DEUTSCHLAND GmbH Oberbrühlstraße 16-18 87700 Memmingen Germany
1.5. Manufacturer(s) of the active substance(s) Active substance L-(+)-lactic acid Name of manufacturer PURAC Bioquimica SA Address of manufacturer Gran Vial 19-25 8160 Montmelo - Barcelona Spain Location of manufacturing sites PURAC Bioquimica SA Gran Vial 19-25 8160 Montmelo - Barcelona Spain PURAC BIOCHEM BV Arkelsedijk 46 4206 AC Gorinchem Netherlands (the) Purac Sínteses Ltda Av. Rui Barbosa, 521 CEP 28015-520 Campos dos Goytacazes - RJ Brazil Purac America Inc. 650 Industrial Park Drive, P.O. Box 38 NE 68008 Blair United States (the) Purac (Corbion) Thailand Ltd Tambol Huay Pong, Amphoe Muang 21150 Rayong Thailand Active substance L-(+)-lactic acid Name of manufacturer Jungbunzlauer S.A. Address of manufacturer Z.I. Portuaire BP 32 67390 Marckolsheim France Location of manufacturing sites Z.I. Portuaire BP 32 67390 Marckolsheim France
2. PRODUCT FAMILY COMPOSITION AND FORMULATION
2.
2.1. Qualitative and quantitative information on the composition of the family Common name IUPAC name Function CAS number EC number Content (%) L-(+)-lactic acid active substance 79-33-4 201-196-2 8,4 - 8,4 % (w/w) Sodium p-cumenesulphonate Non-active substance 15763-76-5 239-854-6 1,32 - 1,32 % (w/w) Sodium 2-ethylhexyl sulfate Non-active substance 126-92-1 204-812-8 0 - 2,1 % (w/w) Diethanolamine Non-active substance 111-42-2 203-868-0 3,92 - 4,234 % (w/w)
2.2. Type(s) of formulation Formulation type(s) AL Any other liquid
PART II SECOND INFORMATION LEVEL - META SPC(S)
1. META SPC 1 ADMINISTRATIVE INFORMATION
1.
1.1. Meta SPC 1 identifier Identifier Meta SPC: meta SPC 1 - Dipping, foaming, spraying ready to use products
1.2. Suffix to the authorisation number Number 1-1
1.3. Product type(s) Product type(s) PT03: Veterinary hygiene
2. META SPC 1 COMPOSITION
2.
2.1. Qualitative and quantitative information on the composition of the meta SPC 1 Common name IUPAC name Function CAS number EC number Content (%) L-(+)-lactic acid active substance 79-33-4 201-196-2 8,4 - 8,4 % (w/w) Sodium p-cumenesulphonate Non-active substance 15763-76-5 239-854-6 1,32 - 1,32 % (w/w) Diethanolamine Non-active substance 111-42-2 203-868-0 4,234 - 4,234 % (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 H319: Causes serious eye irritation. Precautionary statements P264: Wash hands thoroughly after handling. P280: Wear eye protection. P280: Wear face protection. P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P337+P313: If eye irritation persists: Get medical attention. P337+P313: If eye irritation persists: Get medical advice.
4. AUTHORISED USE(S) OF THE META SPC
4.
4.1. Table 1 Disinfection of teats of milk producing animals by manual or automated dipping, foaming or spraying after milking
Use description Product type PT03: Veterinary hygiene Where relevant, an exact description of the authorised use - Target organism(s) (including development stage) Scientific name: no data Common name: Bacteria Development stage: no data Scientific name: no data Common name: Yeasts Development stage: no data Field(s) of use indoor use Manual or automated disinfection of teats of milk producing animals by dipping, foaming or spraying after milking Application method(s) Method: Dipping, foaming or spraying Detailed description: Dipping cup, foaming cup, teat sprayer, automated dipping machine, automated foaming machine or automated spraying machine. Application rate(s) and frequency Application rate: application rate per animal: - cows and buffaloes 3 to 10 ml (5 to 8 ml recommended) - sheep 1,5 to 5 ml (1,5 to 3 ml recommended) - goats 2,5 to 6 ml (2,5 to 4 ml recommended) Dilution (%): Ready to use product Number and timing of application: Contact time : 5 minutes Frequency: 2 to 3 times per day Category(ies) of users professional Pack sizes and packaging material HDPE (High Density Polyethylene) jerrycans 5, 10, 22, 25 and 30 litre HDPE barrel 60 litre HDPE drums 120 and 220 litre HDPE container 640 and 1000 litre
4.1.1. Use-specific instructions See general directions for use of meta SPC 1
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
5. GENERAL DIRECTIONS FOR USE OF THE META SPC 1
5.
5.1. Instructions for use Fill the dipping/foaming cup/sprayer manually or automatically with the ready to use product. Manual or automatic dipping/foaming/spraying on animal’s teats on the full length of the teat after milking. Make sure that the teats are fully covered with disinfectant. Leave the product until next milking. Keep the animals standing for at least 5 minutes until the product has dried. At the next milking, use the teat cleaning and wiping method systematically before attaching the milking cluster. Avoid contact with eyes. Wash hands after work. Product must be brought to a temperature between 20°C and 30°C before use.
5.2. Risk mitigation measures Wear chemical goggles or face protection consistent with European Standard EN ISO 16321 or equivalent. For manual application by spraying: Wear protective chemical resistant gloves consistent with European Standard EN ISO 374 during product handling phase. 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 INHALED: If symptoms occur call a POISON CENTRE or a doctor. IF SWALLOWED: Rinse mouth. Give something to drink, if exposed person is able to swallow. Do NOT induce vomiting. Call a POISON CENTRE or a doctor. IF ON SKIN: Wash skin with water. If symptoms occur call a POISON CENTRE or a doctor. IF IN EYES: Rinse with water. Remove contact lenses, if present and easy to do. Continue rinsing for 5 minutes. Call a POISON CENTRE or a doctor. Refer to the safety data sheet available for professional user: it contains an emergency phone number. Large spillage: Mark out, soak up with an inert absorbant and pump in an emergency tank. Never return spills in original containers for re-use. Keep in suitable, properly labelled and closed containers for disposal.
5.4. Instructions for safe disposal of the product and its packaging At the end of the treatment, dispose unused product and the packaging in accordance with local requirements. Used product can be flushed to the municipal sewer or disposed to the manure deposit depending on local requirements. Avoid release to an individual waste water treatment plant. The paper towels used for removing the product and drying the teats are disposed in the normal domestic waste.
5.5. Conditions of storage and shelf-life of the product under normal conditions of storage Shelf life: 2 years in HDPE
6. OTHER INFORMATION Full titles of EN standards and legislation referred to in section 5.2: EN ISO 374 – Protective gloves against dangerous chemicals and micro-organisms. EN ISO 16321 – Eye and face protection for occupational use.
7. THIRD INFORMATION LEVEL: INDIVIDUAL PRODUCTS IN THE META SPC 1
7.
7.1. Trade name(s), authorisation number and specific composition of each individual product Trade name(s) NATIDINE Market area: EU Bonimal H Lactiliquid Market area: EU LACTILIQ Market area: EU MilchsäureDip-Spray Market area: EU NATILAC Market area: EU PRIMAMO Market area: EU RBT LACTIC Market area: EU ROBOSPRAY LACTIC Market area: EU SPRAYLAC Market area: EU Bonimal CARE LactiLiquid Market area: EU Authorisation number EU-0031195-0001 1-1 Common name IUPAC name Function CAS number EC number Content (%) L-(+)-lactic acid active substance 79-33-4 201-196-2 8,4 Sodium p-cumenesulphonate Non-active substance 15763-76-5 239-854-6 1,32 Diethanolamine Non-active substance 111-42-2 203-868-0 4,234
1. META SPC 2 ADMINISTRATIVE INFORMATION
1.
1.1. Meta SPC 2 identifier Identifier Meta SPC: meta SPC 2 - Dipping ready to use products
1.2. Suffix to the authorisation number Number 1-2
1.3. Product type(s) Product type(s) PT03: Veterinary hygiene
2. META SPC 2 COMPOSITION
2.
2.1. Qualitative and quantitative information on the composition of the meta SPC 2 Common name IUPAC name Function CAS number EC number Content (%) L-(+)-lactic acid active substance 79-33-4 201-196-2 8,4 - 8,4 % (w/w) Sodium p-cumenesulphonate Non-active substance 15763-76-5 239-854-6 1,32 - 1,32 % (w/w) Sodium 2-ethylhexyl sulfate Non-active substance 126-92-1 204-812-8 0 - 2,1 % (w/w) Diethanolamine Non-active substance 111-42-2 203-868-0 3,92 - 3,92 % (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 H319: Causes serious eye irritation. Precautionary statements P264: Wash hands thoroughly after handling. P280: Wear eye protection. P280: Wear face protection. P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P337+P313: If eye irritation persists: Get medical attention. P337+P313: If eye irritation persists: Get medical advice.
4. AUTHORISED USE(S) OF THE META SPC
4.
4.1. Table 1 Disinfection of teats of milk producing animals by manual or automated dipping after milking
Use description Product type PT03: Veterinary hygiene Where relevant, an exact description of the authorised use - Target organism(s) (including development stage) Scientific name: no data Common name: Bacteria Development stage: no data Scientific name: no data Common name: Yeasts Development stage: no data Field(s) of use indoor use Manual or automated disinfection of teats of milk producing animals by dipping after milking Application method(s) Method: Dipping Detailed description: Dipping cup or automated dipping machine. Application rate(s) and frequency Application rate: application rate per animal: - cows and buffaloes 3 to 10 ml (5 ml recommended) - sheep 1,5 to 5 ml (1,5 ml recommended) - goats 2,5 to 6 ml (2,5 ml recommended) Dilution (%): Ready to use product Number and timing of application: Contact time : 5 minutes Frequency: 2 to 3 times per day Category(ies) of users professional Pack sizes and packaging material HDPE (High Density Polyethylene) jerrycans 5, 10, 22, 25 and 30 litre HDPE barrel 60 litre HDPE drums 120 and 220 litre HDPE container 640 and 1000 litre
4.1.1. Use-specific instructions See general directions for use of meta SPC 2
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
5. GENERAL DIRECTIONS FOR USE OF THE META SPC 2
5.
5.1. Instructions for use Fill the dipping cup manually or automatically with the ready to use product. Apply by dipping manually or automatically on animal’s teats on the full length of the teat after milking. Make sure that the teats are fully covered with disinfectant. Leave the product until next milking. Keep the animals standing for at least 5 minutes until the product has dried. At the next milking, use the teat cleaning and wiping method systematically before attaching the milking cluster. Avoid contact with eyes. Wash hands after work. Product must be brought to a temperature between 20°C and 30°C before use.
5.2. Risk mitigation measures Wear chemical goggles or face protection consistent with European Standard EN ISO 16321 or equivalent. 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 INHALED: If symptoms occur call a POISON CENTRE or a doctor. IF SWALLOWED: Rinse mouth. Give something to drink, if exposed person is able to swallow. Do NOT induce vomiting. Call a POISON CENTRE or a doctor. IF ON SKIN: Wash skin with water. If symptoms occur call a POISON CENTRE or a doctor. IF IN EYES: Rinse with water. Remove contact lenses, if present and easy to do. Continue rinsing for 5 minutes. Call a POISON CENTRE or a doctor. Refer to the safety data sheet available for professional user: it contains an emergency phone number. Large spillage: Mark out, soak up with an inert absorbant and pump in an emergency tank. Never return spills in original containers for re-use. Keep in suitable, properly labelled and closed containers for disposal.
5.4. Instructions for safe disposal of the product and its packaging At the end of the treatment, dispose unused product and the packaging in accordance with local requirements. Used product can be flushed to the municipal sewer or disposed to the manure deposit depending on local requirements. Avoid release to an individual waste water treatment plant. The paper towels used for removing the product and drying the teats are disposed in the normal domestic waste.
5.5. Conditions of storage and shelf-life of the product under normal conditions of storage Shelf life: 2 years in HDPE Store below 30°C
6. OTHER INFORMATION Full titles of EN standards and legislation referred to in section 5.2: EN ISO 16321 – Eye and face protection for occupational use.
7. THIRD INFORMATION LEVEL: INDIVIDUAL PRODUCTS IN THE META SPC 2
7.
7.1. Trade name(s), authorisation number and specific composition of each individual product Trade name(s) FILMADINE LL Market area: EU Authorisation number EU-0031195-0002 1-2 Common name IUPAC name Function CAS number EC number Content (%) L-(+)-lactic acid active substance 79-33-4 201-196-2 8,4 Sodium p-cumenesulphonate Non-active substance 15763-76-5 239-854-6 1,32 Diethanolamine Non-active substance 111-42-2 203-868-0 3,92
7.2. Trade name(s), authorisation number and specific composition of each individual product Trade name(s) FILMADINE LC Market area: EU FILMADINE C Market area: EU Bonimal H Lactidip C Market area: EU CERTI CREME C Market area: EU CERTI FILM C Market area: EU COSMADINE C Market area: EU DIPLAC C Market area: EU EQUO LACTO C Market area: EU FILMADIP C Market area: EU FILMALAC C Market area: EU FILMALINE C Market area: EU FILMATREMP C Market area: EU FILMORANGE C Market area: EU FP FILM C Market area: EU HY-COSMETIC C Market area: EU HYPREDIP PLUS C Market area: EU INO EXTRA C Market area: EU INO FILM C Market area: EU LACTIDIP C Market area: EU MilchsäureFilmdip-Super C Market area: EU PRIMASKIN C Market area: EU SUPREMADINE C Market area: EU ZOO FILM RED C Market area: EU Authorisation number EU-0031195-0003 1-2 Common name IUPAC name Function CAS number EC number Content (%) L-(+)-lactic acid active substance 79-33-4 201-196-2 8,4 Sodium p-cumenesulphonate Non-active substance 15763-76-5 239-854-6 1,32 Sodium 2-ethylhexyl sulfate Non-active substance 126-92-1 204-812-8 2,1 Diethanolamine Non-active substance 111-42-2 203-868-0 3,92
7.3. Trade name(s), authorisation number and specific composition of each individual product Trade name(s) FILMADINE Market area: EU Bonimal H Lactidip Market area: EU CERTI CREME + Market area: EU CERTI FILM Market area: EU COSMADINE Market area: EU DIPLAC Market area: EU EQUO LACTO Market area: EU FILMADIP Market area: EU FILMALAC Market area: EU FILMALINE Market area: EU FILMATREMP Market area: EU FILMORANGE Market area: EU FP FILM Market area: EU HY-COSMETIC Market area: EU HYPREDIP PLUS Market area: EU INO EXTRA Market area: EU INO FILM Market area: EU LACTIDIP Market area: EU MilchsäureFilmdip-Super Market area: EU PRIMASKIN Market area: EU SUPREMADINE Market area: EU ZOO FILM RED Market area: EU LAURACTIV Market area: EU Salus TOP Market area: EU LAURAFILM Market area: EU Juvelit-extreme Market area: EU Bonimal CARE LactiDip Market area: EU Authorisation number EU-0031195-0004 1-2 Common name IUPAC name Function CAS number EC number Content (%) L-(+)-lactic acid active substance 79-33-4 201-196-2 8,4 Sodium p-cumenesulphonate Non-active substance 15763-76-5 239-854-6 1,32 Sodium 2-ethylhexyl sulfate Non-active substance 126-92-1 204-812-8 2,1 Diethanolamine Non-active substance 111-42-2 203-868-0 3,92
Versions
Cited by
- Commission Implementing Regulation (EU) 2025/1171 of 16 June 2025 granting a Union authorisation for the biocidal product family PRODHYNET’s Lactic acid based products in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance) Regulation · Grade B
On 26 April 2019, PRODHYNET SA submitted an application to the European Chemicals Agency (the Agency) in accordance with Article 43(1) of Regulation (EU) No 528/2012 and Article 4 of Commission Implementing Regulation (EU) No 414/2013 for Union authorisation of the same biocidal product family, as referred to in Article 1 of Implementing Regulation (EU) No 414/2013, named PRODHYNET's Lactic acid based products, of product-type 3, as described in Annex V to Regulation (EU) No 528/2012. The application was recorded under case number BC-XX051283-02 in the Register for Biocidal Products. The appli