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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 540/2011 ,
Reg. (EU) No 787/2011
Old Legislation 2008/941/EC
Date of approval 01/01/2012 Expiration of approval 31/12/2021
RMS

Co-RMS
HU

FR
Risk Assessment EFSA
Category PG Review Report   Confirmatory data 2016
  Approval 2011
Authorisation at national level
Authorised in In progress for
AT, BE, CY, CZ, DE, EL, FR, HR, IE, IT, NL, PT, UK ES, MT, SI
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • 1-Naphthylacetamide and 1-naphthylacetic acid (sum of 1-naphthylacetamide and 1-naphthylacetic acid and its salts, expressed as 1-naphythlacetic acid)
    MRLs Annex II
Classification Reg. 1272/2008
Skin Corr. 1A - H314 Eye Irrit. 2 - H319
Toxicological information
Reference values Source Remark
ADI 0.1 EFSA 11  
ARfD 0.1 EFSA 11  
AOEL 0.07 EFSA 11  
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