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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 05/57/EC ,
Reg. (EU) 2018/1262 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) No 2017/1511 ,
Reg. (EU) No 762/2013
Date of approval 01/05/2006 Expiration of approval 31/10/2019
RMS

Co-RMS
PL

NL
Risk Assessment Commission
Category HB Review Report
Remarks The original RMS was Italy.

Extension of approval period: Reg. (EU) 2017/1511
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, MT, NL, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • MCPA and MCPB (MCPA, MCPB including their salts, esters and conjugates expressed as MCPA) (F) (R)
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Skin Irrit. 2 - H315
Eye Dam. 1 - H318 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.05 SCoFCAH July 08  
ARfD 0.15 Dir 05/57  
AOEL 0.04 Dir 05/57  
Other
ARfD 0.01 AUS 1994 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level