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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/69 ,
Reg. (EU) No 1100/2011 ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2009 Expiration of approval 31/12/2018
RMS

Co-RMS
DK

RO
Risk Assessment EFSA
Category HB Review Report   Confirmatory data 2016
  Inclusion 2008
Remarks Substance fulfilling criteria Annex V Reg 1490/2002
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, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Dicamba
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Eye Dam. 1 - H318
Aquatic Chronic 3 - H412  
Toxicological information
Reference values Source Remark
ADI 0.3 Dir 08/69  
ARfD 0.3 Dir 08/69  
AOEL 0.3 Dir 08/69  
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