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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 05/58/EC ,
Reg. (EU) 2018/917 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) 2017/841
Date of approval 01/12/2005 Expiration of approval 31/07/2019
RMS

Co-RMS
DE

NL
Risk Assessment Commission
Category IN Review Report
Remarks The original RMS was the Netherlands.
Authorisation at national level
Authorised in In progress for
AT, BE, CY, CZ, DE, DK, EL, ES, FR, IT, LU, MT, NL, PL, PT, RO, SE, SI HU
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Milbemectin (sum of milbemycin A4 and milbemycin A3, expressed as milbemectin)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Acute Tox. 4 - H332
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.03 05/58/EC  
ARfD 0.03 05/58/EC  
AOEL 0.014 05/58/EC  
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