Label: NOXZEMA ANTIBLEMISH- salicylic acid cloth

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Updated December 5, 2022

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  • NOXZEMA ULTIMATE CLEAR ANIT-BLEMISH PADS - (Salicylic Acid) lotion

  • Drug Facts

    Active ingredient


    Salicylic Acid (2.0% )

  • Purpose

    Acne treatment

  • Uses

    • For the treatment of acne
    • Dries up acne pimples
    • Helps prevent new acne pimples
  • Warnings

    • For external use only.
    • Flammable - keep away from fire or flame.
    • When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occues, only use one topical acne medication at a time.

    • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
  • Directions

    • Clean the skin thoroughly before applying product
    • Cover the entire affected area with a thin layer and rinse thoroughly one to three times daily
    • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily, if needed or as directed by a doctor.
    • If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
    • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
  • Inactive ingredients

    Alcohol Denat., Water (Aqua), PEG-4, PPG-11 Stearyl Ether, Fragrance (Parfum), Camphor, Eucalyptus Globulus Leaf Oil, Menthol, Disodium EDTA, Benzyl Alcohol, Benzyl Benzoate, Cinnamal, Citral, Eugenol, Geraniol, Geraniol, Limonene, Linalool.

  • Questions?

    1-800-436-4361

  • Packaging

    Noxzema Anti-Blemish Pads

  • INGREDIENTS AND APPEARANCE
    NOXZEMA  ANTIBLEMISH
    salicylic acid cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1259
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.02 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CINNAMALDEHYDE (UNII: SR60A3XG0F)  
    GERANIOL (UNII: L837108USY)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    BENZYL BENZOATE (UNII: N863NB338G)  
    EUGENOL (UNII: 3T8H1794QW)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    WATER (UNII: 059QF0KO0R)  
    POLYETHYLENE GLYCOL 200 (UNII: R95B8J264J)  
    PPG-11 STEARYL ETHER (UNII: S4G2J0Y0LG)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ALCOHOL (UNII: 3K9958V90M)  
    MENTHOL (UNII: L7T10EIP3A)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
    CITRAL (UNII: T7EU0O9VPP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1259-10.0284 g in 1 PACKET; Type 0: Not a Combination Product09/01/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D09/01/2012
    Labeler - Conopco Inc. (001375088)
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