Label: PHISODERM ANTI-BLEMISH GEL CLEANSER- salicylic acid gel

  • NDC Code(s): 10742-8417-1
  • Packager: The Mentholatum Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

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

    • avoid contact with the 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, then gently massage onto skin
    • Rinse well and pat dry
    • use twice daily
  • Inactive ingredients

    water, lauramidopropyl betaine, sodium C14-16 olefin sulfonate, lauryl glucoside, trolamine, butylene glycol, chamomilla recutita (matricaria) flower extract, disodium EDTA, DMDM hydantoin, fragrance, glycerin, hydroxyphenyl propamidobenzoic acid, iodopropynyl butylcarbamate, lactic acid, pentylene glycol, polysorbate 20, sodium chloride

  • Questions?

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

  • Principal Display Panel

    Phisoderm Anti-Blemish Gel Cleanser
  • Principal Display Panel

    Phisoderm Anti-Blemish Gel Cleanser
  • INGREDIENTS AND APPEARANCE
    PHISODERM ANTI-BLEMISH GEL CLEANSER 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-8417
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CHAMOMILE (UNII: FGL3685T2X)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10742-8417-1177 g in 1 TUBE; Type 0: Not a Combination Product09/01/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00609/01/2013
    Labeler - The Mentholatum Company (002105757)
    Registrant - The Mentholatum Company (002105757)
    Establishment
    NameAddressID/FEIBusiness Operations
    The Mentholatum Company002105757manufacture(10742-8417)
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