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Dimethenamid-P Approved
Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
| Legislation |
03/84/EC
, Reg. (EU) 2018/1262 , Reg. (EU) No 540/2011 , Reg. (EU) No 823/2012 |
Old Legislation |
Reg. (EU) 2016/950
, Reg. (EU) 2017/1511 |
|---|---|---|---|
| Date of approval | 01/01/2004 | Expiration of approval | 31/10/2019 |
| RMS
Co-RMS |
DE
BG |
Risk Assessment | Commission |
| Category | HB | Review Report |
List of Studies 2017
Inclusion 2003 |
| Remarks | Extension of the approval period: Reg. (EU) 207/1511 | ||
Authorisation at national level
| Authorised in | In progress for |
|---|---|
| AT, BE, BG, CZ, DE, EL, ES, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SI, SK, UK | FI |
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
| Legislation | Annexes |
|---|---|
|
Classification Reg. 1272/2008
| Acute Tox. 4 - H302 | Skin Sens. 1 - H317 |
| Aquatic Acute 1 - H400 | Aquatic Chronic 1 - H410 |
Toxicological information
| Reference values | Source | Remark | |
|---|---|---|---|
| ADI | 0.02 | 03/84/EC | |
| ARfD | 0.25 | 03/84/EC | |
| AOEL | 0.04 | 03/84/EC | |
| Other | |||
| ADI 0.07, ARfD 0.5 JMPR 2005 | |||
- Legend
-
- RMS:Rapporteur Member State
- Co-RMS:Co-Rapporteur Member State
- ADI:Acceptable daily intake
- ARfD:Acute reference dose
- AOEL:Acceptable operator exposure level