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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2006/74/EC ,
Reg. (EU) No 1166/2013 ,
Reg. (EU) No 2018/524 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) No 878/2014
Date of approval 01/06/2007 Expiration of approval 30/04/2019
RMS

Co-RMS
IE

PL
Risk Assessment EFSA
Category HB Review Report   Inclusion 2006
  Conditions of approval 2013
Remarks Extention of the approval (Reg (EU)2018/524)
The original RMS was Denmark.
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, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Dichlorprop (Sum of dichlorprop (including dichlorprop-P), its salts, esters and conjugates, expressed as dichlorprop (R)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Skin Irrit. 2 - H315
Skin Sens. 1 - H317 Eye Dam. 1 - H318
Toxicological information
Reference values Source Remark
ADI 0.06 Dir 06/74  
ARfD 0.5 Dir 06/74  
AOEL 0.35 Dir 06/74  
Other
 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level