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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 06/64/EC ,
Reg. (EU) No 2018/524 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) No 678/2014
Date of approval 01/05/2007 Expiration of approval 30/04/2019
RMS

Co-RMS
FR

BG
Risk Assessment EFSA
Category FU Review Report
Remarks Extention of the approval (Reg (EU) 2018/524)
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
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, SE, SI, SK, UK
Classification Reg. 1272/2008
Skin Sens. 1 - H317 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.03 Dir 06/64  
ARfD Not applicable Dir 06/64  
AOEL 0.03 Dir 06/64  
Other
ARfD unnecessary ADI 0,03 JMPR 2003 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level