See Full Document Text
Official Journal EN
of the European Union L series
2025/474 17.3.2025
COMMISSION IMPLEMENTING REGULATION (EU) 2025/474
of 13 March 2025
granting a Union authorisation for the single biocidal product ‘Büfa-Oxy WS’ 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 29 April 2024, BÜFA Cleaning GmbH & Co. KG 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(2) for Union authorisation of the same single biocidal product, as
referred to in Article 1 of Implementing Regulation (EU) No 414/2013, named ‘Büfa-Oxy WS’, of product-types 2
and 4, as described in Annex V to Regulation (EU) No 528/2012. The application referred to the single biocidal
product ‘CLARMARIN® 350’ (authorisation number EU-0028964-0005), which is a part of the related reference
biocidal product family ‘Evonik’s Hydrogen Peroxide Product Family’. The application was recorded under case
number BC-AN094539-21 in the Register for Biocidal Products. The application also indicated the authorisation
number of the related reference biocidal product family ‘Evonik's Hydrogen Peroxide Product Family’ authorised by
Commission Implementing Regulation (EU) 2023/2183(3), with authorisation number EU-0028964-0000.
(2) The single biocidal product ‘Büfa-Oxy WS’ contains hydrogen peroxide 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-types 2
and 4.
(3) On 29 July 2024, the Agency submitted to the Commission its opinion(4)and the draft summary of the biocidal
product characteristics (‘SPC’) of ‘Büfa-Oxy WS’ in accordance with Article 6 of Implementing Regulation (EU)
No 414/2013 and Article 44(4) of Regulation (EU) No 528/2012.
(1) OJ L 167, 27.6.2012, p. 1, ELI: http://data.europa.eu/eli/reg/2012/528/oj.
(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, ELI: http://data.europa.eu/eli/reg_impl/2013/414/oj).
(3) Commission Implementing Regulation (EU) 2023/2183 of 18 October 2023 granting a Union authorisation for the biocidal product
family ‘Evonik’s Hydrogen Peroxide Product Family’ in accordance with Regulation (EU) No 528/2012 of the European Parliament and
of the Council (OJ L, 2023/2183, 19.10.2023, ELI: http://data.europa.eu/eli/reg_impl/2023/2183/oj).
(4) European Chemicals Agency opinion of 29 July 2024 on the Union authorisation of the same single biocidal product ‘Büfa-Oxy WS’,
https://echa.europa.eu/opinions-on-union-authorisation.
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(4) In its opinion, the Agency concludes that the proposed differences between the single biocidal product ‘Büfa-Oxy
WS’ and the related single biocidal product ‘CLARMARIN® 350’, which is a part of the related reference biocidal
product family ‘Evonik's Hydrogen Peroxide Product Family’, are limited to information which can be the subject of
an administrative change in accordance with Commission Implementing Regulation (EU) No 354/2013(5), and that
based on the assessment of the related reference biocidal product family ‘Evonik's Hydrogen Peroxide Product Family’
and subject to compliance with the draft SPC, the same single biocidal product ‘Büfa-Oxy WS’ meets the conditions
laid down in Article 19(1) of Regulation (EU) No 528/2012.
(5) 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 ‘Büfa-Oxy WS’.
(6) The expiry date of the authorisation should be aligned with the expiry date of the authorisation of the related
reference biocidal product family ‘Evonik's Hydrogen Peroxide Product Family’.
(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-0033025-0000 is hereby granted to BÜFA Cleaning GmbH & Co.
KG for the making available on the market and use of the same single biocidal product ‘Büfa-Oxy WS’ in accordance with
the summary of the biocidal product characteristics set out in the Annex.
The Union authorisation is valid from 6 April 2025until 31 October 2033.
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, 13 March 2025.
For the Commission
The President
Ursula VON DER LEYEN
(5) 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).
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ANNEX
Summary of product characteristics for a biocidal product
Büfa-Oxy WS
Product type(s)
PT02: Disinfectants and algaecides not intended for direct application to humans or animals
PT04: Food and feed area
Authorisation number: EU-0033025-0000
R4BP asset number: EU-0033025-0000
1. ADMINISTRATIVE INFORMATION
1.1. Trade name(s) of the product
Trade name(s) Büfa-Oxy WS
O 33
1.2. Authorisation holder
Name BÜFA Cleaning GmbH & Co. KG
Name and address of the authorisation holder
Address August-Hanken-Straße 30 26125 Oldenburg DE
Authorisation number EU-0033025-0000
R4BP asset number EU-0033025-0000
Date of the authorisation 6 April 2025
Expiry date of the authorisation 31 October 2033
1.3. Manufacturer(s) of the product
Name of manufacturer Evonik Antwerpen NV
Address of manufacturer Tijsmanstunnel West 2040 Antwerpen Belgium
Location of manufacturing sites Evonik Antwerpen NV
Tijsmanstunnel West 2040 Antwerpen Belgium
Name of manufacturer Evonik Operations GmbH
Address of manufacturer Rellinghauser Straße 1-11 45128 Essen Germany
Location of manufacturing sites Evonik Operations GmbH
Untere Kanalstr. 3 79618 Rheinfelden Germany
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Name of manufacturer Evonik Peroxid GmbH
Address of manufacturer Industriestraße 1 9721 Weißenstein Austria
Location of manufacturing sites Evonik Peroxid GmbH
Industriestraße 1 9721 Weißenstein Austria
Name of manufacturer Evonik Peroxide Netherlands BV
Address of manufacturer Hettenheuvelweg 37 /39 1101 BM Amsterdam
Netherlands (the)
Location of manufacturing sites Evonik Peroxide Netherlands BV
Oosterhorn 14 9936 HD Farmsum Netherlands (the)
Name of manufacturer Evonik España y Portugal SA
Address of manufacturer Afueras s/n 50784 La Zaida Spain
Location of manufacturing sites Evonik España y Portugal SA
C/ Afueras s/n. 50784 La Zaida Spain
1.4. Manufacturer(s) of the active substance(s)
Active substance Hydrogen peroxide
Name of manufacturer Evonik Antwerpen NV
Address of manufacturer Tijsmanstunnel West 2040 Antwerpen Belgium
Location of manufacturing sites Evonik Antwerpen NV
Tijsmanstunnel West 2040 Antwerpen Belgium
Active substance Hydrogen peroxide
Name of manufacturer Evonik Operations GmbH
Address of manufacturer Rellinghauser Straße 1-11 45128 Essen Germany
Location of manufacturing sites Evonik Operations GmbH
Untere Kanalstr. 3 79618 Rheinfelden Germany
Active substance Hydrogen peroxide
Name of manufacturer Evonik Peroxid GmbH
Address of manufacturer Industriestraße 1 9721 Weißenstein Austria
Location of manufacturing sites Evonik Peroxid GmbH
Industriestraße 1 9721 Weißenstein Austria
Active substance Hydrogen peroxide
Name of manufacturer Evonik Peroxide Netherlands BV
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Address of manufacturer Hettenheuvelweg 37 /39 1101 BM Amsterdam
Netherlands (the)
Location of manufacturing sites Evonik Peroxide Netherlands BV
Oosterhorn 14 9936 HD Farmsum Netherlands (the)
Active substance Hydrogen peroxide
Name of manufacturer Evonik España y Portugal SA
Address of manufacturer Afueras s/n 50784 La Zaida Spain
Location of manufacturing sites Evonik España y Portugal SA
C/ Afueras s/n. 50784 La Zaida Spain
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 (%)
Hydrogen active substance 7722-84-1 231-765-0 35 % (w/w)
peroxide
2.2. Type(s) of formulation
SL Soluble concentrate
3. HAZARD AND PRECAUTIONARY STATEMENTS
Hazard statements H302: Harmful if swallowed.
H315: Causes skin irritation.
H318: Causes serious eye damage.
H335: May cause respiratory irritation.
H412: Harmful to aquatic life with long lasting effects.
H272: May intensify fire; oxidiser.
Precautionary statements P261: Avoid breathing vapours.
P264: Wash hands thoroughly after handling.
P270: Do not eat, drink or smoke when using this
product.
P271: Use only outdoors or in a well-ventilated area.
P273: Avoid release to the environment.
P280: Wear protective clothing / eye protection / face
protection.
P301+P312: IF SWALLOWED: Call a POISON CENTER /
doctor / physician if you feel unwell.
P330: Rinse mouth.
P302+P352: IF ON SKIN: Wash with plenty of water/
soap.
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P304+P340: IF INHALED: Remove person to fresh air and
keep comfortable for breathing.
P312: Call a POISON CENTER/doctor/physician if you
feel unwell.
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.
P332+P313: If skin irritation occurs: Get medical advice.
P403+P233: Store in a well-ventilated place. Keep
container tightly closed.
P405: Store locked up.
P501: Dispose of contents in accordance with local
requirements.
P501: Dispose of container in accordance with local
requirements.
P210: Keep away from heat, hot surfaces, sparks, open
flames and other ignition sources. No smoking.
P220: Keep away from clothing or other combustible
materials.
P370+P378: In case of fire: Use water to extinguish.
4. AUTHORISED USE(S)
4.1. Use description
Table 1.
Laundry disinfection in closed washing machines by dosing
Product type PT02: Disinfectants and algaecides not intended for direct application
to humans or animals
Where relevant, an exact description of the -
authorised use
Target organism(s) (including development Common name: bacteria
stage) Development stage: -
Common name: yeasts
Development stage: -
Common name: viruses
Development stage: -
Common name: fungi
Development stage: -
Field(s) of use indoor use
Laundry disinfection in washing machines.
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Application method(s) Method: Loading (dosing)
Detailed description:
The product is automatically dosed into the closed washing machine
during the washing process (main wash).
Application rate(s) and frequency Application rate: 0,019 – 0,029% (w/w) hydrogen peroxide. The
biocidal products are diluted accordingly in order to achieve an in-use
concentration in the range of 0,019 – 0,029% (w/w). For example, in
the case of 35% (w/w) hydrogen peroxide product: 0,5 ml or 0,75 ml
concentrate add water up to 1 litre to achieve 0,019% (w/w) or
0,029% (w/w). For products with different concentrations of
hydrogen peroxide the values have to be adjusted accordingly.
Number and timing of application:
Frequency: Daily / if required
Bacteria, yeasts, fungi: In use concentration 0,019% (w/w) hydrogen
peroxide in the wash solution.
Alkaline buffering agent: 0,6 ml/l BEIPUR ANP.
Contact time: 10 minutes
Temperature: 70°C
Viruses: In use concentration 0,029% (w/w) hydrogen peroxide in the
wash solution.
Alkaline buffering agent: 0,6 ml/l BEIPUR ANP
Contact time: 10 minutes
Temperature: 80°C
Cloth: liquid ratio = 1:4
Category(ies) of users professional
Pack sizes and packaging material HDPE bottle 1, 5 litres
HDPE jerry can 10, 20, 30, 60 litres
HDPE drum 200 litres
HDPE container 1000 litres
HDPE ISO tank 20m3
4.1.1. Use-specific instructions
The product and alkaline buffering agent (BEIPUR ANP) are automatically dosed into the closed washing machine
during the washing process. The dosing of both components, i.e. the biocidal product and the alkaline buffering
agent BEIPUR ANP, is realised via two separate pipes and dosing stations. Biocidal product and alkaline buffering
agent should not be mixed prior the dosing into the washing machine. Treatment Interval - daily / if required (0,5
hours / day).
4.1.2. Use-specific risk mitigation measures
Wear chemical resistant goggles consistent with European Standard EN 16321 or equivalent, protective clothing
chemically resistant to the biocidal product, chemical resistant gloves classified under the European Standard EN
374 or equivalent, face shield and RPE (APF = 10 ) during mixing and loading. Glove and coverall material to be
specified by the authorisation holder within the product information. See section 6 for the full titles of the EN
standards.
This is without prejudice to the application of Council Directive 98/24/EC and other Union legislation in the area of
health and safety at work. See section 6 for the full reference to Council Directive 98/24/EC .
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Technical RMM: Local exhaust ventilation (50 %) and good standard of general ventilation (3 ACH). Observe label
instructions.
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
No use specific 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
No use specific 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
No use specific instructions of storage and shelf-life of the product under normal conditions of storage. See general
directions for use.
4.2. Use description
Table 2
Disinfection of distribution system for drinking water by cleaning in place (CIP)
Product type PT04: Food and feed area
Where relevant, an exact description of the -
authorised use
Target organism(s) (including development Common name: bacteria
stage) Development stage: -
Common name: yeasts
Development stage: -
Common name: fungi
Development stage: -
Field(s) of use indoor use
Disinfection of distributing and storing installations for drinking
water.
Application method(s) Method: CIP (Cleaning in place) in closed systems
Detailed description:
Disinfecting the interior surfaces of closed systems by CIP
Application rate(s) and frequency Application rate: 4,7 % (w/w ) hydrogen peroxide For disinfection of
bacteria, yeasts and fungi the product should be diluted to 4,7% (w/w)
hydrogen peroxide. For example, in the case of a product containing
35% (w/w) hydrogen peroxide: add 114 ml product to 819 ml water
to achieve a dilution of 4,7% (w/w) hydrogen peroxide. For products
with different concentrations of hydrogen peroxide the values have to
be adjusted accordingly.
Number and timing of application:
Contact time: at least 3 hours
Frequency: Daily / if required
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Temperature: room temperature
Category(ies) of users professional
Pack sizes and packaging material HDPE bottle 1, 5 litres
HDPE jerry can 10, 20, 30, 60 litres
HDPE drum 200 litres
HDPE container 1000 litres
HDPE ISO tank 20m3
4.2.1. Use-specific instructions
CIP (Cleaning in place): Clean prior to disinfection. Circulate the diluted product through the system under
conditions of increased turbulence and flow velocity. After 3 hours contact time, pipelines and tanks are rinsed
with water before refilled with drinking water. For disinfection of bacteria, yeasts and fungi the product should be
diluted to 4,7% (w/w) hydrogen peroxide.
For example, for a product containing 35% (w/w) hydrogen peroxide: add 114 ml product to 819 ml water to
achieve a dilution of 4,7% (w/w) hydrogen peroxide. For products with different concentrations of hydrogen
peroxide the values have to be adjusted accordingly.
4.2.2. Use-specific risk mitigation measures
Wear chemical resistant goggles consistent with European Standard EN 16321 or equivalent, protective clothing
chemically resistant to the biocidal product, chemical resistant gloves classified under the European Standard EN
374 or equivalent, face shield and RPE (APF = 10) during mixing and loading. See section 6 for the full titles of the
EN standards.
Glove and coverall material to be specified by the authorisation holder within the product information.
This is without prejudice to the application of Council Directive 98/24/EC and other Union legislation in the area of
health and safety at work. See section 6 for the full reference to Council Directive 98/24/EC.
Technical RMM: Local exhaust ventilation (50 %) and good standard of general ventilation (3 ACH). Observe label
instructions.
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
No use specific 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
No use specific instructions for safe disposal of the product and its packaging. See general directions for use.
4.2.5. Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage
No use specific instructions of storage and shelf-life of the product under normal conditions of storage. See general
directions for use.
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4.3. Use description
Table 3
Disinfection of non-porous hard surfaces and equipment by immersion
Product type PT04: Food and feed area
Where relevant, an exact description of the -
authorised use
Target organism(s) (including development Common name: bacteria
stage) Development stage: -
Common name: yeasts
Development stage: -
Common name: fungi
Development stage: -
Field(s) of use indoor use
Equipment in both food and drink industries, large scale catering
kitchens and large scale canteens.
Application method(s) Method: Open system: immersion
Detailed description:
Manual immersion of equipment in closed baths. Automated
immersion of equipment in closed baths.
Application rate(s) and frequency Application rate: 8,1% (w/w) hydrogen peroxide. For disinfection of
bacteria, yeasts and fungi the product should be diluted to 8,1% (w/w)
hydrogen peroxide. For example, for a product containing 35% (w/w)
hydrogen peroxide: add 200 ml product to 738 ml water to achieve a
dilution of 8,1% (w/w) hydrogen peroxide. For products with
different concentrations of hydrogen peroxide the values have to be
adjusted accordingly.
Number and timing of application:
Contact time: 60 minutes
Frequency: Daily / if required
Temperature: room temperature
Category(ies) of users professional
Pack sizes and packaging material HDPE bottle 1, 5 litres
HDPE jerry can 10, 20, 30, 60 litres
HDPE drum 200 litres
HDPE container 1000 litres
HDPE ISO tank 20m3
4.3.1. Use-specific instructions
For disinfection of bacteria yeasts and fungi the product should be diluted to 8,1% (w/w) hydrogen peroxide. For
example, for a product containing 35% (w/w) hydrogen peroxide: add 200 ml product to 738 ml water to achieve a
dilution of 8,1% (w/w) hydrogen peroxide. For products with different concentrations of hydrogen peroxide the
values have to be adjusted accordingly.
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Immersion: Equipment in the food and feed industry is disinfected by immersion. Pre-clean the equipment. The
disinfection solution should be diluted into vats (i.e. pouring or pumping the product into vats). The equipment to
be disinfected is manually or automatically placed into these vats (closed baths) and taken out after a contact time of
not less than 60 minutes. After the disinfection procedure is completed, equipment is rinsed with water. The
disinfection of the immersion/dipping bath should be replaced after each disinfection cycle.
4.3.2. Use-specific risk mitigation measures
Wear chemical resistant goggles consistent with European Standard EN 16321 or equivalent, protective clothing
chemically resistant to the biocidal product, chemical resistant gloves classified under the European Standard EN
374 or equivalent, face shield and RPE (APF = 10) during mixing and loading and application. Glove and coverall
material to be specified by the authorisation holder within the product information. See section 6 for the full titles
of the EN standards.
This is without prejudice to the application of Council Directive 98/24/EC and other Union legislation in the area of
health and safety at work. See section 6 for the full reference to Council Directive 98/24/EC. No access to the room is
permitted during disinfection without wearing adequate PPE and RPE as described above.
Technical RMM: Local exhaust ventilation (50 %) and good standard of general ventilation (3 ACH). Dipping bath has
to be placed in a separate room. For use only in areas inaccessible to the general public. Professional users without
PPE and RPE (APF=10) are not allowed to enter the disinfection room. Keep the bath closed during disinfection,
only open to load and discharge.
Observe label instructions.
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
No use specific first aid instructions and emergency measures to protect the environment. See general directions
for use.
4.3.4. Where specific to the use, the instructions for safe disposal of the product and its packaging
No use specific instructions for safe disposal of the product and its packaging. See general directions for use.
4.3.5. Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage
No use specific instructions of storage and shelf-life of the product under normal conditions of storage. See general
directions for use.
4.4. Use description
Table 4
Disinfection of surfaces by cleaning in place (CIP)
Product type PT04: Food and feed area
Where relevant, an exact description of the -
authorised use
Target organism(s) (including development Common name: bacteria
stage) Development stage: -
Common name: yeasts
Development stage: -
Common name: fungi
Development stage: -
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Field(s) of use indoor use
Disinfection of food contact inner surfaces of pipe work and tank
systems in food and feed industry.
Application method(s) Method: CIP in closed systems
Detailed description:
Disinfecting the interior surfaces of closed systems by Cleaning In
Place (CIP).
Application rate(s) and frequency Application rate: 4,7% (w/w) hydrogen peroxide. For disinfection of
bacteria, yeasts and fungi the product should be diluted to 4,7% (w/w)
hydrogen peroxide. For example, for a product containing 35% (w/w)
hydrogen peroxide: add 114 ml product to 819 ml water to achieve a
dilution of 4,7% (w/w) hydrogen peroxide. For products with
different concentrations of hydrogen peroxide the values have to be
adjusted accordingly.
Number and timing of application:
Contact time: at least 3 hours
Frequency: Daily / if required
Temperature: room temperature
Category(ies) of users professional
Pack sizes and packaging material HDPE bottle 1, 5 litres
HDPE jerry can 10, 20, 30, 60 litres
HDPE drum 200 litres
HDPE container 1000 litres
HDPE ISO tank 20m3
4.4.1. Use-specific instructions
Clean prior to disinfection. The inner surfaces of pipe work and tank systems are disinfected by CIP process. For
disinfection of bacteria yeasts and fungi the product should be diluted to 4,7% (w/w) hydrogen peroxide. For
example, for a product containing 35% (w/w) hydrogen peroxide: add 114 ml product to 819 ml water to achieve a
dilution of 4,7% (w/w) hydrogen peroxide. For products with different concentrations of hydrogen peroxide the
values have to be adjusted accordingly.
The process is carried out by circulating the disinfection solution through the system under conditions of increased
turbulence and flow velocity. The application is automated and a closed process. After 3 hours contact time,
pipelines and tanks are rinsed with water under closed system conditions as well.
4.4.2. Use-specific risk mitigation measures
Wear chemical resistant goggles consistent with European Standard EN 16321 or equivalent, protective clothing
chemically resistant to the biocidal product, chemical resistant gloves classified under the European Standard EN
374 or equivalent, face shield and RPE (APF =10) during mixing and loading. See section 6 for the full titles of the
EN standards.
Glove and coverall material to be specified by the authorisation holder within the product information.
This is without prejudice to the application of Council Directive 98/24/EC and other Union legislation in the area of
health and safety at work. See section 6 for the full reference to Council Directive 98/24/EC.
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Technical RMM: Local exhaust ventilation (50 %) and good standard of general ventilation (3 ACH). Observe label
instructions.
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
No use specific first aid instructions and emergency measures to protect the environment. See general directions
for use.
4.4.4. Where specific to the use, the instructions for safe disposal of the product and its packaging
No use specific instructions for safe disposal of the product and its packaging. See general directions for use.
4.4.5. Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage
No use specific instructions 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
See use specific instructions for each use.
5.2. Risk mitigation measures
See use specific risk mitigation measures for each use.
Observe label instructions.
5.3. Particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the
environment
First aid instructions
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. Information to Healthcare personnel/doctor: Initiate
life support measures if needed, thereafter call a POISON CENTRE.
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.
IF INHALED: Move to fresh air and keep at rest in a position comfortable for breathing.
If symptoms: Call 112/ambulance for medical assistance.
If no symptoms: Call a POISON CENTRE or a doctor.
Accidental release measures
Large spillage: Collect product in suitable containers (for example made of plastic) using appropriate equipment (for
example liquid pump) for disposal. Never return spills in original containers for re-use. Keep away from flammable
and incompatible substances. Rinse away any residue with plenty of water. Dispose of absorbed material in
accordance with the applicable environmental regulations.
Small spillage: Dilute product with lots of water and rinse away or absorb with liquid-binding material (for example
diatomaceous earth or universal binder). Pick up mechanically and collect in suitable containers. Clean contaminated
surface thoroughly. Pack and label wastes like the product. Do not detach label from the delivery containers prior to
disposal.
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5.4. Instructions for safe disposal of the product and its packaging
At the end of the treatment, dispose of unused product and the packaging in accordance with local requirements.
Used product can be flushed to municipal sewer depending on local requirements.
5.5. Conditions of storage and shelf-life of the product under normal conditions of storage
Advice on protection against fire and explosion
Store away from direct sunlight and heat sources.
Store away from sources of ignition - No smoking.
Store away from flammable substances.
Store away from incompatible substances.
Storage
Temperature requirement- during storage maximum 40 °C and protect from frost.
Store in clean, dry and well- ventilated places.
Transport and store container in upright position only.
Always close container tightly after removal of product.
Avoid leakage and residues of the product on the containers.
Advice on common storage
Do not store together with alkalis, reductants, metallic salts (risk of decomposition).
Do not store together with organic solvents (risk of explosion).
Shelf-life:
24 months
6. OTHER INFORMATION
The full titles of the EN standards referenced in the “Use-specific mitigation measures” sections are:
EN 16321 - Eye and face protection for occupational users
EN 374 – Protective gloves against chemicals and micro-organisms
The Council Directive referenced in the “Use-specific mitigation measures” sections is: Council Directive 98/24/EC of
7 April 1998on the protection of the health and safety of workers from the risks related to chemical agents at work
(fourteenth individual Directive within the meaning of Article 16(1) of Directive 89/391/EEC) (OJ L 131, 5.5.1998
[RMJ1] , p.11).
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(1) Instructions for use, risk mitigation measures and other directions for use under this section are valid for any authorised uses.
14/14 ELI: http://data.europa.eu/eli/reg_impl/2025/474/oj