Label: OXY DAILY DEFENSE EXFOLIATING FACE SCRUB- salicylic acid gel

  • NDC Code(s): 10742-8306-1
  • Packager: The Mentholatum Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 01/13

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

  • Active ingredient

    Salicylic acid 2%

    Close
  • Purpose

    Acne treatment

    Close
  • Uses

    treats and helps prevent acne

    Close
  • Warnings

    For external use only

    When using this product

    keep away from eyes. If contact occurs, flush thoroughly with water.
    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.

    If pregnant or breast-feeding

    ask a health professional before use.

    Close
  • Keep Out of Reach of Children

    If swallowed, get medical help or contact a Poison Control Center right away.

    Close
  • Directions

    wet face
    squeeze scrub into hands and massage gently over face and neck
    rinse thoroughly and pat dry
    because too much drying of the skin may occur, start with 1 use, then gradually increase to 2 or 3 times daily if needed or as directed by a doctor
    if bothersome dryness or peeling occurs, reduce usage to once a day or every other day
    Close
  • Inactive ingredients

    acrylates copolymer, aloe barbadensis leaf juice, aluminum powder, anhydrous citric acid, astragalus membranaceus root extract, butyl methoxydibenzoylmethane, caprylyl glycol, cocamidopropyl betaine, D&C violet no. 2, edetate disodium, ethylhexyl palmitate, ethylhexyl salicylate, ethylhexyl methoxycinnamate, FD&C blue no. 1, forsythia suspensa fruit extract, fragrance, glycerin, PEG-40 hydrogenated castor oil, PEG-8/SMDI copolymer, petrolatum, phenoxyethanol, polyethylene, potassium C12-13 alkyl phosphate, potassium sorbate, PPG-26-buteth-26, purified water, silica, sodium benzoate, sodium C14-16 olefin sulfonate, sorbic acid, trolamine

    Close
  • Questions?

    1-877-636-2677 MON-FRI 9 AM-5 PM (EST)

    Close
  • Package/Label Principal Display Panel
  • INGREDIENTS AND APPEARANCE
    OXY DAILY DEFENSE EXFOLIATING FACE SCRUB 
    salicylic acid gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-8306
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALUMINUM (UNII: CPD4NFA903)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)  
    AVOBENZONE (UNII: G63QQF2NOX)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    D&C VIOLET NO. 2 (UNII: 350KA7O6HK)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    OCTISALATE (UNII: 4X49Y0596W)  
    OCTINOXATE (UNII: 4Y5P7MUD51)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FORSYTHIA SUSPENSA FRUIT (UNII: P4793M1ES5)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    PEG-8/SMDI COPOLYMER (UNII: CCX72L6NY6)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)  
    WATER (UNII: 059QF0KO0R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    SORBIC ACID (UNII: X045WJ989B)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:10742-8306-1 142 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333D 01/15/2013
    Labeler - The Mentholatum Company (002105757)
    Close