Label: OXY VOLCANIC ASH ACNE FACE WASH- salicylic acid liquid

  • NDC Code(s): 10742-8334-1
  • Packager: The Mentholatum Company
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 17, 2024

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  • Active ingredient

    Salicylic acid 2%

  • Purpose

    Acne treatment

  • Uses

    treats and helps prevent acne blemishes

  • 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

    Keep out of reach of children.

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

  • Directions

    • wet face gently
    • gently massage cleanser onto skin, avoiding eye area
    • rinse thoroughly
  • Inactive ingredients

    acrylates copolymer, aloe barbadensis leaf juice, anhydrous citric acid, butylene glycol, charcoal powder, cocamidopropyl betaine, edetate disodium, fragrance, glycerin, menthol, portulaca oleracea extract, potassium C12-13 alkyl phosphate, potassium sorbate, purified water, silica, sodium benzoate, sodium C14-16 olefin sulfonate, trolamine, volcanic ash

  • Questions?

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

  • Package/Label Principal Display Panel

    Oxy Volcanic Ash Acne Wash
  • Principal Display Panel

    Drug Facts
  • INGREDIENTS AND APPEARANCE
    OXY VOLCANIC ASH ACNE FACE WASH 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-8334
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
    PURSLANE (UNII: M6S840WXG5)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    WATER (UNII: 059QF0KO0R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10742-8334-1207 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00611/01/2018
    Labeler - The Mentholatum Company (002105757)
    Registrant - The Mentholatum Company (002105757)
    Establishment
    NameAddressID/FEIBusiness Operations
    The Mentholatum Company002105757manufacture(10742-8334)
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