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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/116 ,
Reg. (EU) 2017/195 ,
Reg. (EU) No 540/2011
   
Date of approval 01/08/2009 Expiration of approval 31/07/2022
RMS NL

Risk Assessment EFSA
Category HB Review Report   Specification 2009
  Confirmatory data 2012
Remarks Co-RMS is Norway
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, CY, CZ, DE, DK, EE, EL, ES, FI, FR, IT, LT, LU, LV, NL, SE, SK UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Aclonifen
    MRLs Annex II
Classification Reg. 1272/2008
Skin Sens. 1A - H317 Carc. 2 - H351
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.07 Dir 08/116  
ARfD Not applicable Dir 08/116  
AOEL 0.07 Dir 08/116  
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