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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
IT

ES
Risk Assessment EFSA
Category HB Review Report
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
FR, IT, PT, SK ES
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Oxadiazon
    MRLs Annex IIIA
Classification Reg. 1272/2008
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.0036 EFSA 2010  
ARfD 0.12 EFSA 2010  
AOEL 0.05 EFSA 2010  
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