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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2016/2016 ,
Reg. (EU) 84/2018 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012
Old Legislation 03/70/EC
Date of approval 01/06/2004 Expiration of approval 31/01/2019
RMS

Co-RMS
UK

IE
Risk Assessment Commission
Category HB Review Report   List of Studies 2018
  Review Report 2003
Remarks Extension of the approval period (Reg. (EU) 84/2018)

The original RMS was Denmark.
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Mecoprop (sum of mecoprop-p and mecoprop expressed as mecoprop)
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Eye Dam. 1 - H318
Aquatic Chronic 2 - H411  
Toxicological information
Reference values Source Remark
ADI 0.01 Dir 03/70  
ARfD Not applicable Dir 03/70  
AOEL 0.04 Dir 03/70  
Other
ARfD 0.04 AUS 2001 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level