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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 06/10/EC ,
Reg. (EU) 2018/1262 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) No 2017/1511 ,
Reg. (EU) No 533/2013
Date of approval 01/04/2006 Expiration of approval 31/10/2019
RMS

Co-RMS
FR

ES
Risk Assessment Commission
Category IN Review Report   List of Studies 2017
  Draft review report 2005
Remarks The original RMS was the Netherlands.

Extension of approval period: Reg. (EU) 2017/1511
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
Acute Tox. 3 - H301 Skin Sens. 1B - H317
Acute Tox. 4 - H332 STOT RE 1 - H372
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.006 06/10/EC  
ARfD 0.125 06/10/EC  
AOEL 0.004 06/10/EC  
Other
ADI 0,01 ARfD 0,1 JMPR 2005 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level