Commission Implementing Regulation (EU) 2023/1143 of 9 June 2023 granting a Union authorisation for the single biocidal product ‘Chemisept IPA-N’ in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance)
Date: 2023-06-09
Institutions: Directorate-General for Health and Food Safety, European Commission
Subjects: biocide, chemical product, cosmetic product, decontamination, market approval








L_2023151EN.01001101.xml










12.6.2023   


EN


Official Journal of the European Union


L 151/11








            COMMISSION IMPLEMENTING REGULATION (EU) 2023/1143
of 9 June 2023
         
granting a Union authorisation for the single biocidal product ‘Chemisept IPA-N’ 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 2012 concerning the making available on the market and use of biocidal products (1), and in particular Article 44(5), first subparagraph, thereof,

Whereas:







(1)


On 24 April 2019, AS Chemi-Pharm submitted to the European Chemicals Agency (‘the Agency’) an application in accordance with Article 43(1) of Regulation (EU) No 528/2012 and Article 4 of Commission Implementing Regulation (EU) No 414/2013 (2) for authorisation of the same single biocidal product, as referred to in Article 1 of that Regulation, named ‘Chemisept IPA-N’, of product-type 1, as described in Annex V to Regulation (EU) No 528/2012. The application was recorded under case number BC-UU051173-14 in the Register for Biocidal Products (‘the Register’). The application also indicated the application number of the related reference biocidal product family ‘Knieler & Team Propanol Family’, recorded in the Register under case number BC-AQ050985-22.












(2)


The same single biocidal product ‘Chemisept IPA-N’ contains propan-1-ol and propan-2-ol as the active substances, which are included in the Union list of approved active substances referred to in Article 9(2) of Regulation (EU) No 528/2012 for product-type 1.












(3)


On 8 December 2021, the Agency submitted to the Commission an opinion (3) and the draft summary of the biocidal product characteristics (‘SPC’) of ‘Chemisept IPA-N’ in accordance with Article 6 of Implementing Regulation (EU) No 414/2013.












(4)


The opinion concludes that the proposed differences between the same single biocidal product and the related reference biocidal product are limited to information which can be the subject of an administrative change in accordance with Commission Implementing Regulation (EU) No 354/2013 (4), and that based on the assessment of the related reference biocidal product family ‘Knieler & Team Propanol Family’ and subject to compliance with the draft SPC, the same single biocidal product meets the conditions laid down in Article 19(1) of Regulation (EU) No 528/2012.












(5)


On 24 October 2022, the Agency transmitted to the Commission the draft SPC in all the official languages of the Union in accordance with Article 44(4) of Regulation (EU) No 528/2012.












(6)


The Commission concurs with the opinion of the Agency and considers it therefore appropriate to grant a Union authorisation for the same single biocidal product ‘Chemisept IPA-N’.












(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-0027678-0000 is granted to AS Chemi-Pharm for the making available on the market and use of the same single biocidal product ‘Chemisept IPA-N’ in accordance with the summary of the biocidal product characteristics set out in the Annex.
The Union authorisation is valid from 2 July 2023 until 31 July 2032.


Article 2
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union.




This Regulation shall be binding in its entirety and directly applicable in all Member States.
Done at Brussels, 9 June 2023.


For the Commission


The President

Ursula VON DER LEYEN
            





(1)  
            OJ L 167, 27.6.2012, p. 1.

(2)  Commission Implementing Regulation (EU) No 414/2013 of 6 May 2013 specifying a procedure for the authorisation of same biocidal products in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (OJ L 125, 7.5.2013, p. 4).

(3)  ECHA opinion for ‘Chemisept IPA-N’, 8 December 2021, https://echa.europa.eu/opinions-on-union-authorisation

(4)  Commission Implementing Regulation (EU) No 354/2013 of 18 April 2013 on changes of biocidal products authorised in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (OJ L 109, 19.4.2013, p. 4).




ANNEX

Summary of product characteristics for a biocidal product

Chemisept IPA-N
Product type 1 – Human hygiene (Disinfectants)
Authorisation number: EU-0027678-0000
R4BP asset number: EU-0027678-0000
1.   ADMINISTRATIVE INFORMATION

1.1.   Trade name(s) of the product







Trade name(s)


Chemisept IPA-N




1.2.   Authorisation holder








Name and address of the authorisation holder


Name


Chemi-Pharm AS




Address


Tänassilma tee 11, 76406 Tänassilma küla, Saku vald Estonia




Authorisation number


EU-0027678-0000





R4BP asset number



EU-0027678-0000




Date of the authorisation


2.7.2023




Expiry date of the authorisation


31.7.2032




1.3.   Manufacturer(s) of the product







Name of manufacturer


AS Chemi-Pharm




Address of manufacturer


Tänassilma tee 11, 76406 Tänassilma küla, Saku vald, Harju maakond Estonia




Location of manufacturing sites


AS Chemi-Pharm, Tänassilma tee 11, 76406 Tänassilma küla, Saku vald, Harju maakond Estonia




1.4.   Manufacturer(s) of the active substance(s)







Active substance


Propan-1-ol




Name of manufacturer


OQ Chemicals GmbH (formerly Oxea GmbH)




Address of manufacturer


Rheinpromenade 4a, 40789 Monheim am Rhein Germany




Location of manufacturing sites


OQ Chemicals Corperation (formerly Oxea Coperation), 2001 FM 3057 TX, 77414 Bay City United States













Active substance


Propan-1-ol




Name of manufacturer


BASF SE




Address of manufacturer


Carl-Bosch-Str. 38, 67056 Ludwigshafen Germany




Location of manufacturing sites


BASF SE, Carl-Bosch-Str. 38, 67056 Ludwigshafen Germany













Active substance


Propan-1-ol




Name of manufacturer


SASOL Chemie GmbH & Co. KG




Address of manufacturer


Secunda Chemical Operations, Sasol Place, 50 Katherine Street, 2090 Sandton South Africa




Location of manufacturing sites


Secunda Chemical Operations, PDP Kruger Street, 2302 Secunda South Africa













Active substance


Propan-2-ol




Name of manufacturer


INEOS Solvent Germany GmbH




Address of manufacturer


Römerstrasse 733, 47443 Moers Germany




Location of manufacturing sites


INEOS Solvent Germany GmbH, Römerstrasse 733, 47443 Moers Germany
INEOS Solvent Germany GmbH, Shamrockstrasse 88, 44623 Herne Germany




2.   PRODUCT COMPOSITION AND FORMULATION

2.1.   Qualitative and quantitative information on the composition of the product











Common name


IUPAC name


Function


CAS number


EC number


Content (%)




Propan-1-ol


 


Active Substance


71-23-8


200-746-9


30,0 




Propan-2-ol


 


Active Substance


67-63-0


200-661-7


45,0 




2.2.   Type of formulation

AL – Any other liquid
3.   HAZARD AND PRECAUTIONARY STATEMENTS







Hazard statements


Flammable liquid and vapour.
Causes serious eye damage.
May cause drowsiness or dizziness.
Repeated exposure may cause skin dryness or cracking.




Precautionary statements


Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. – No smoking.
Keep container tightly closed.
Avoid breathing vapours.
Use only outdoors or in a well-ventilated area.
IF INHALED:Remove person to fresh air and keep comfortable for breathing.
IF IN EYES:Rinse cautiously with water for several minutes.Remove contact lenses, if present and easy to do. Continue rinsing.
Immediately call a POISON CENTER/doctor.
Store in a well-ventilated place.Keep cool.
Store locked up.
Dispose of container to an authorised waste collection point.




4.   AUTHORISED USE(S)

4.1.   Use description


Table 1


Use # 1 – hygienic handrub, liquid







Product type


PT01 – Human hygiene (Disinfectants)




Where relevant, an exact description of the authorised use


Not relevant




Target organism(s) (including development stage)


Scientific name: no data
Common name: Bacteria
Development stage: no data
Scientific name: no data
Common name: Mycobacteria
Development stage: no data
Scientific name: no data
Common name: Yeasts
Development stage: no data
Scientific name: no data
Common name: Enveloped viruses
Development stage: no data




Field(s) of use


Indoor






—


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) Contact time: 30 s
Dilution (%): 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, 125, 500, 1 000  ml in transparent/white high-density polyethylene (HDPE) bottles with polypropylene (PP) flip top caps;
5 000  ml transparent/white HDPE canister with HDPE screwed 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.
Do not refill.
4.1.2.   Use-specific risk mitigation measures

See general directions for use.
4.1.3.   Where specific to the use, the particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment

See general directions for use.
4.1.4.   Where specific to the use, the instructions for safe disposal of the product and its packaging

See general directions for use.
4.1.5.   Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage

See general directions for use.
4.2.   Use description


Table 2


Use # 2 – surgical handrub, liquid







Product type


PT01 – Human hygiene (Disinfectants)




Where relevant, an exact description of the authorised use


Not relevant




Target organism(s) (including development stage)


Scientific name: no data
Common name: Bacteria
Development stage: no data
Scientific name: no data
Common name: Mycobacteria
Development stage: no data
Scientific name: no data
Common name: Yeasts
Development stage: no data
Scientific name: no data
Common name: enveloped viruses
Development stage: no data




Field(s) of use


Indoor
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: Rub sufficient amount in portions of 3 ml (use dispensers: for example set to 1,5 ml per stroke, 2 strokes per 3 ml). Contact time: 90 s
Dilution (%): 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, 125, 500, 1 000  ml in transparent/white high-density polyethylene (HDPE) bottles with polypropylene (PP) flip top caps;
5 000  ml transparent/white HDPE canister with HDPE screwed 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.
Do not refill.
4.2.2.   Use-specific risk mitigation measures

See general directions for use.
4.2.3.   Where specific to the use, the particulars of likely direct or indirect effects, first aid instructions and emergency measures to protect the environment

See general directions for use.
4.2.4.   Where specific to the use, the instructions for safe disposal of the product and its packaging

See general directions for use.
4.2.5.   Where specific to the use, the conditions of storage and shelf-life of the product under normal conditions of storage

See general directions for use.
5.   GENERAL DIRECTIONS FOR USE (1)

5.1.   Instructions for use

For professional use only.
5.2.   Risk mitigation measures

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

First-aid measures general: Move the affected person away from the contaminated area. Get medical advice/attention if you feel unwell. If possible, show this sheet.
IF INHALED: Move to fresh air and keep at rest in a position comfortable for breathing. Call a POISON CENTRE or a doctor.
IF ON SKIN: Immediately wash skin with plenty of water. Thereafter take off all contaminated clothing and wash it before reuse. Continue to wash the skin with water for 15 minutes. Call a POISON CENTRE or a doctor.
IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing for at least 15 minutes. Call 112/ambulance for medical assistance.
Information to Healthcare personnel/doctor:
The eyes should also be rinsed repeatedly on the way to the doctor if eye exposure to alkaline chemicals (pH > 11), amines and acids like acetic acid, formic acid or propionic acid.
IF SWALLOWED: Immediately rinse mouth. Give something to drink, if exposed person is able to swallow. Do NOT induce vomiting. Call 112/ambulance for medical assistance.
Accidental release measures:
Stop leak if safe to do so. Remove ignition sources. Use special care to avoid static electric charges. No open flames. No smoking.
Prevent entry to sewers and public waters.
Wipe up with absorbent material (for example cloth). Soak up spills with inert solids, such as clay or diatomaceous earth as soon as possible. Take up mechanically (sweeping, shovelling). Dispose of in accordance with relevant local regulations.
5.4.   Instructions for safe disposal of the product and its packaging

Disposal must be done according to official regulations. Do not empty into drains. Do not dispose of with domestic waste. Dispose of contents/container to an authorised waste collection point. Empty the packaging completely prior to disposal. When totally empty, containers are recyclable like any other packing.
5.5.   Conditions of storage and shelf-life of the product under normal conditions of storage

Shelf-life: 24 months
Store in dry, cool, well-ventilated area. Keep container tightly closed. Keep out of direct sunlight.
Recommended storage temperature: 0– 30 °C
Do not store at temperatures below 0 °C
Do not store near food, drink and animal feedingstuff. Keep away from combustible material.
6.   OTHER INFORMATION



(1)  Instructions for use, risk mitigation measures and other directions for use under this section are valid for any authorised uses.