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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 06/85/EC ,
Reg. (EU) 2018/917 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) No 2015/415
Date of approval 01/08/2007 Expiration of approval 31/07/2019
RMS

Co-RMS
NL

PL
Risk Assessment EFSA
Category PG Review Report
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, RO, SE, SI, SK, UK
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Acute Tox. 3 - H311
Skin Corr. 1C - H314 Acute Tox. 4 - H332
Aquatic Chronic 2 - H411  
Toxicological information
Reference values Source Remark
ADI 0.03 Dir 06/85  
ARfD 0.05 SCoFCAH Dec.08  
AOEL 0.03 Dir 06/85  
Other
ARfD 0,05 - ADI 0,05 JMPR 2002 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level