A more recent version of this regulatory record is available. This version is kept only as a historical record. Please see the Record history section for link to the most recent version.
List details
Basic info
Status | Opinion Adopted |
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Submitter | Norway |
Regulatory programme |
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Classification
Proposed harmonised classification by the dossier submitter |
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Hazard classes open for commenting | Physical hazards Health hazards (except Aspiration Hazard) Environmental hazards (except Hazardous to the Ozone Layer) |
Proposed specific concentration limits by the dossier submitter | SCL Skin sensitisation: 0,001%. SCL skin irritation: 0,01% |
Intention timeline
Date of intention | 2016-01-05 |
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Expected date of submission | 2016-02-29 |
Submitted for accordance check | 2016-03-18 |
Final submission date | 2018-01-15 |
Start of consultation | 2018-02-12 |
Deadline for commenting | 2018-04-13 |
Date of opinion | 2018-11-30 |
Legal deadline for opinion adoption | 2019-07-17 |
Documents
CLH report |
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Comments received |
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Public consultations - received attachments |
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RAC opinion |
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Background document |
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Related substances
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Record history
The following timeline shows when we detected changes of this regulatory record (the date might slightly differ from the date of the actual change). Additions between versions are hightlighted in green color, red color shows data removed between versions.
April 4, 2019
- Regulatory programme: BPD → Active substance in Biocidal Products
Oct. 29, 2020
- CLP Annex VI Index Number: 613-335-00-8
Dec. 10, 2021
- ATP number and date: ATP15 - (19/05/2020), 01/03/2022
- Link to ATP / File Title: Official Journal
- Link to ATP / Full Path: https://eur-lex.europa.eu/legal-content/EN/TXT/?qid=1598259094155&uri=CELEX:32020R1182
This version
Feb. 18, 2019
- Background document: https://echa.europa.eu/documents/10162/a9d0b194-afe3-71b0-3978-6df14513cdf5
- Comments received: https://echa.europa.eu/documents/10162/40eb5dd7-7796-0306-e581-0319654652b5 → https://echa.europa.eu/documents/10162/ff274308-f09e-04c1-ba68-0534e3193216
- RAC opinion: https://echa.europa.eu/documents/10162/c5397851-ef29-13b1-24ae-a213c967ad38
Dec. 11, 2018
- Date of opinion: 2018-11-30
- Status: Opinion Development → Opinion Adopted
Dec. 4, 2018
- Regulatory programme: Existing active substance in Biocidal Products (in the meaning of Directive 98/8/EC) → BPD
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