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IBUPROFEN

  • UNII: WK2XYI10QM
  • Formula: C13H18O2
  • Preferred Substance Name: IBUPROFEN
  • InChIKey: HEFNNWSXXWATRW-UHFFFAOYSA-N

  • 15687-27-1
  • 239-784-6
  • (+/-)-2-(P-ISOBUTYLPHENYL)PROPIONIC ACID
  • (+/-)-IBUPROFEN
  • (+/-)-P-ISOBUTYLHYDRATROPIC ACID
  • ACHES-N-PAIN
  • ADVIL
  • ADVIL ALLERGY SINUS COMPONENT IBUPROFEN
  • ADVIL CONGESTION RELIEF COMPONENT IBUPROFEN
  • BENZENEACETIC ACID, .ALPHA.-METHYL-4-(2-METHYLPROPYL)-
  • BENZENEACETIC ACID, .ALPHA.-METHYL-4-(2-METHYLPROPYL), (+/-)-
  • BURANA
  • CALDOLOR
  • CAP-PROFEN
  • CHILDREN'S ADVIL COLD COMPONENT IBUPROFEN
  • CHILDREN'S MOTRIN COLD COMPONENT IBUPROFEN
  • COMBOGESIC COMPONENT IBUPROFEN
  • COMBUNOX COMPONENT IBUPROFEN
  • IB-100
  • IBU
  • IBUPRIN
  • IBUPROFEN [EMA EPAR]
  • IBUPROFEN [EP MONOGRAPH]
  • IBUPROFEN [HSDB]
  • IBUPROFEN [INCI]
  • IBUPROFEN [INN]
  • IBUPROFEN [JAN]
  • IBUPROFEN [MART.]
  • IBUPROFEN [MI]
  • IBUPROFEN [ORANGE BOOK]
  • IBUPROFEN [USAN]
  • IBUPROFEN [USP IMPURITY]
  • IBUPROFEN [USP MONOGRAPH]
  • IBUPROFEN [USP-RS]
  • IBUPROFEN [VANDF]
  • IBUPROFEN [WHO-DD]
  • IBUPROFEN [WHO-IP]
  • IBUPROFEN COMPONENT OF ADVIL ALLERGY SINUS
  • IBUPROFEN COMPONENT OF ADVIL CONGESTION RELIEF
  • IBUPROFEN COMPONENT OF CHILDREN'S ADVIL COLD
  • IBUPROFEN COMPONENT OF CHILDREN'S MOTRIN COLD
  • IBUPROFEN COMPONENT OF COMBOGESIC
  • IBUPROFEN COMPONENT OF COMBUNOX
  • IBUPROFEN COMPONENT OF REPREXAIN
  • IBUPROFEN COMPONENT OF SINE-AID IB
  • IBUPROFEN COMPONENT OF VICOPROFEN
  • IBUPROFENUM [WHO-IP LATIN]
  • IBUPROHM
  • IBU-TAB
  • M01AE01
  • MEDIPREN
  • MIDOL
  • MOTRIN
  • NSC-256857
  • NUPRIN
  • PEDEA
  • PROFEN
  • RD 13621
  • REPREXAIN COMPONENT IBUPROFEN
  • RUFEN
  • SINE-AID IB COMPONENT IBUPROFEN
  • TAB-PROFEN
  • U-18,573
  • U-18573
  • VICOPROFEN COMPONENT IBUPROFEN

Note

UNIIs are generated based on scientific identity characteristics using ISO 11238 data elements. UNII availability does not imply any regulatory review or approval. Synonyms and mappings are based on the best public information available at the time of publication. Please report any problems/errors associated with this data to FDA-SRS@fda.hhs.gov.