Label: NOXZEMA ANTIBLEMISH- salicylic acid cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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.

Drug Label Information

Updated December 12, 2018

If you are a consumer or patient please visit this version.

  • Noxema Ultimate Clear Anti-Blemish Pads

    Drug Facts

  • Active ingredient

    Salicylic acid 2%

  • Purpose

    Acne treatment

  • Uses

    • For the treatment of acne
    • Clears 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 occurs, 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

    • Cleanse the skin thoroughly before applying this product.
    • Cover the entire affected area with a thin layer 1 to 3 times daily.
    • Because excessive drying of the skin may occur, start with 1 application daily, then gradually increase to 2 or 3 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, PEG-4, PPG-11 Stearyl Ether, Eucalyptus Globulus Leaf Oil, Camphor, Menthol, Disodium EDTA, Fragrance.

  • Questions?

    1-800-436-4361

  • PRINCIPAL DISPLAY PANEL - 90 Pad Bottle Label

    PDP 90 Pads PDP Noxzema Anti-Blemish 90 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
    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)  
    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)