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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/127 ,
Reg. (EU) 2017/195 ,
Reg. (EU) No 540/2011
   
Date of approval 01/09/2009 Expiration of approval 31/08/2020
RMS

Co-RMS
SI

SK
Risk Assessment Commission
Category PG Review Report   Update 2012
  Inclusion 2008
Remarks Substance fulfilling criteria Annex VI Reg. 2229/2004
Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, EL, ES, FI, FR, HR, HU, IE, IT, LU, NL, PL, PT, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Gibberellin (++)
    MRLs Annex IV
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.3 Reg. (EU) No 540/2011  
ARfD Not applicable Reg. (EU) No 540/2011  
AOEL 0.18 Reg. (EU) No 540/2011  
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