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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2010/39/EU ,
Reg. (EU) No 540/2011
Old Legislation 2008/69/EC
Date of approval 01/01/2009 Expiration of approval 31/12/2018
RMS

Co-RMS
BE

AT
Risk Assessment EFSA
Category HB Review Report   Confirmatory data 2014
  Revision 2010
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, CY, CZ, DE, EL, ES, FR, HR, HU, IE, IT, LT, NL, PL, PT, RO, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Lenacil
    MRLs Annex IIIA
Classification Reg. 1272/2008
Carc. 2 - H351 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.12 Dir 10/39  
ARfD Not applicable Dir 10/39  
AOEL 0.4 Dir 10/39  
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