Choose the experimental features you want to try

This document is an excerpt from the EUR-Lex website

Document 32025R2200

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

C/2025/6978

OJ L, 2025/2200, 30.10.2025, ELI: http://data.europa.eu/eli/reg_impl/2025/2200/oj (BG, ES, CS, DA, DE, ET, EL, EN, FR, GA, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

Legal status of the document In force

ELI: http://data.europa.eu/eli/reg_impl/2025/2200/oj

European flag

Official Journal
of the European Union

EN

L series


2025/2200

30.10.2025

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 (1), and in particular Article 50(2) thereof,

Whereas:

(1)

On 8 July 2022, Commission Implementing Regulation (EU) 2022/1186 (2) 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 (3) 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 (4) 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


(1)   OJ L 167, 27.6.2012, p. 1, ELI: http://data.europa.eu/eli/reg/2012/528/oj.

(2)  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).

(3)  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).

(4)  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.


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

1.   ADMINISTRATIVE INFORMATION

1.1.   Family name

Name

Propanol 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 holder

Name

Schülke & Mayr GmbH

Address

Robert-Koch-Str. 2 22851 Norderstedt Germany

Authorisation number

 

EU-0027466-00

R4BP asset number

 

EU-0027466-0000

Date of the authorisation

 

31.7.2022

Expiry date of the authorisation

 

30.6.2032


Name of manufacturer

Schülke & Mayr GmbH

Address of manufacturer

Robert-Koch-Str. 2 22851 Norderstedt Germany

Location of manufacturing sites

Schülke & Mayr GmbH site 1 Robert-Koch-Str. 2 22851 Norderstedt Germany


Name of manufacturer

A.F.P. Antiseptica Forschungs- und Produktionsgesellschaft mbH

Address of manufacturer

Otto-Brenner-Straße 16 21337 Lüneburg Germany

Location of manufacturing sites

A.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 substance

Propan-2-ol

Name of manufacturer

INEOS Solvent Germany GmbH

Address of manufacturer

Römerstrasse 733 47443 Moers Germany

Location of manufacturing sites

INEOS Solvent Germany GmbH site 1 INEOS Solvent Germany GmbH, Römerstrasse 733 47443 Moers Germany


Active substance

Propan-2-ol

Name of manufacturer

Ineos Solvents Germany GmbH (formerly Sasol)

Address of manufacturer

Römerstraße 733 47443 Moers Germany

Location of manufacturing sites

Ineos Solvents Germany GmbH (formerly Sasol) site 2 Shamrockstr. 88 44623 Herne Germany


Active substance

Propan-2-ol

Name of manufacturer

Shell Chemicals Europe B.V.

Address of manufacturer

Postbus 2334 3000 CH Rotterdam Netherlands (the)

Location of manufacturing sites

Shell Chemicals Europe B.V. site 1 BV/Shell Nederland Raffinaderij B.V. Vondelingenweg 601 3196 KK Rotterdam-Pernis Netherlands (the)


Active substance

Propan-1-ol

Name of manufacturer

OQ Chemicals GmbH (formerly OXEA)

Address of manufacturer

Rheinpromenade 4a 40789 Monheim am Rhein Germany

Location of manufacturing sites

OQ Chemicals GmbH (formerly OXEA) site 1 OQ Chemicals Corporation, 2001 FM 3057 (formerly OXEA Corporation) TX 77414-2968 Bay City United States (the)


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

Sasol Chemie GmbH & Co. KG site 1 Secunda Chemical Operations, PDP Kruger Street 2302 Secunda South Africa


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 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 name

IUPAC name

Function

CAS number

EC number

Content (%)

Propan-2-ol

 

Active substance

67-63-0

200-661-7

45 - 45 % (w/w)

Propan-1-ol

 

Active substance

71-23-8

200-746-9

30 - 30 % (w/w)

Tetradecanol

Myristil alcohol

Non-active substance

112-72-1

204-000-3

0 - 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)

1.   META SPC 1 ADMINISTRATIVE INFORMATION

1.1.   Meta SPC 1 identifier

Identifier

Meta SPC: meta SPC 1

1.2.   Suffix to the authorisation number

Number

1-1

1.3.   Product type(s)

Product type(s)

PT01: Human hygiene

2.   META SPC 1 COMPOSITION

2.1.   Qualitative and quantitative information on the composition of the meta SPC 1

Common name

IUPAC name

Function

CAS number

EC number

Content (%)

Propan-2-ol

 

Active substance

67-63-0

200-661-7

45 - 45 % (w/w)

Propan-1-ol

 

Active substance

71-23-8

200-746-9

30 - 30 % (w/w)

Tetradecanol

Myristil alcohol

Non-active substance

112-72-1

204-000-3

0,95 - 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 type

PT01: Human hygiene

Where relevant, an exact description of the authorised use

Not 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 material

100 ml, 500 ml and 1 000  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 type

PT01: Human hygiene

Where relevant, an exact description of the authorised use

Not 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 users

professional

Pack sizes and packaging material

100 ml, 500 ml and 1 000  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 protect

Market area: EU

desmanol plus

Market area: EU

desmanol pro

Market area: EU

desmanol ultra

Market area: EU

desmanol clinpure

Market area: EU

desmanol advanced

Market area: EU

desmanol ethanolfree

Market area: EU

desmanol pro pure

Market area: EU

sensiva protect

Market area: EU

virusept protect

Market area: EU

septoderm

Market area: EU

microshield

Market area: EU

Halasept 710

Market area: EU

Authorisation number

 

EU-0027466-0001 1-1

Common name

IUPAC name

Function

CAS number

EC number

Content (%)

Propan-2-ol

 

Active substance

67-63-0

200-661-7

45 % (w/w)

Propan-1-ol

 

Active substance

71-23-8

200-746-9

30 % (w/w)

Tetradecanol

Myristil alcohol

Non-active substance

112-72-1

204-000-3

0,95 % (w/w)

1.   META SPC 2 ADMINISTRATIVE INFORMATION

1.1.   Meta SPC 2 identifier

Identifier

Meta SPC: meta SPC 2

1.2.   Suffix to the authorisation number

Number

1-2

1.3.   Product type(s)

Product type(s)

PT01: Human hygiene

2.   META SPC 2 COMPOSITION

2.1.   Qualitative and quantitative information on the composition of the meta SPC 2

Common name

IUPAC name

Function

CAS number

EC number

Content (%)

Propan-2-ol

 

Active substance

67-63-0

200-661-7

45 - 45 % (w/w)

Propan-1-ol

 

Active substance

71-23-8

200-746-9

30 - 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 type

PT01: Human hygiene

Where relevant, an exact description of the authorised use

Not 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 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 material

100 ml, 500 ml and 1 000  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 type

PT01: Human hygiene

Where relevant, an exact description of the authorised use

Not 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 users

professional

Pack sizes and packaging material

100 ml, 500 ml and 1 000  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 protect

Market area: EU

desmanol pure+

Market area: EU

desmanol pure pro

Market area: EU

desmanol pure guard

Market area: EU

desmanol expert

Market area: EU

desmanol pure ultra

Market area: EU

desmanol EF

Market area: EU

desmanol clear

Market area: EU

sensiva pure

Market area: EU

virusept pure

Market area: EU

septoderm pure

Market area: EU

microshield pure

Market area: EU

Halasept 720

Market area: EU

Authorisation number

 

EU-0027466-0002 1-2

Common name

IUPAC name

Function

CAS number

EC number

Content (%)

Propan-2-ol

 

Active substance

67-63-0

200-661-7

45 % (w/w)

Propan-1-ol

 

Active substance

71-23-8

200-746-9

30 % (w/w)

7.2.   Trade name(s), authorisation number and specific composition of each individual product

Trade name(s)

desmanol pure universal

Market area: EU

desmanol pure plus

Market area: EU

desmanol pure expert

Market area: EU

desmanol proshield

Market area: EU

desmanol healthcare

Market area: EU

desmanol duo

Market area: EU

desmanol EtOH-free

Market area: EU

desmanol zero

Market area: EU

sensiva pure+

Market area: EU

virusept expert

Market area: EU

septoderm pure+

Market area: EU

microshield pure+

Market area: EU

Halasept 740

Market area: EU

Authorisation number

 

EU-0027466-0003 1-2

Common name

IUPAC name

Function

CAS number

EC number

Content (%)

Propan-2-ol

 

Active substance

67-63-0

200-661-7

45 % (w/w)

Propan-1-ol

 

Active substance

71-23-8

200-746-9

30 % (w/w)


ELI: http://data.europa.eu/eli/reg_impl/2025/2200/oj

ISSN 1977-0677 (electronic edition)


Top