Label: PHISODERM ANTI BLEMISH BODY WASH- salicylic acid liquid

  • NDC Code(s): 10742-8451-1
  • 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 on the body and face

  • Warnings

    For external use only

    When using this product

    • avoid contact with 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

    • lather and massage onto skin
    • thoroughly cleanse areas prone to breakouts
    • rinse thoroughly
  • Inactive ingredients

    water, sodium laureth sulfate, disodium cocoamphodiacetate, cocamidopropyl betaine, sodium methyl cocoyl taurate, methyl gluceth-20, glycerin, aloe barbadensis leaf juice, anhydrous citric acid, butylene glycol, chamomilla recutita (matricaria) flower extract, diazolidinyl urea, disodium EDTA, fragrance, hydroxyphenyl propamidobenzoic acid, methylparaben, pentylene glycol, polysorbate 20, propylene glycol, propylparaben, tocopheryl acetate [vitamin E]

  • Questions?

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

  • Principal Display Panel

    Phisoderm Anti-Blemish Body Wash
  • Principal Display Panel

    Phisoderm Anti-Blemish Body Wash
  • INGREDIENTS AND APPEARANCE
    PHISODERM ANTI BLEMISH BODY WASH 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-8451
    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
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)  
    METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    1,2-BUTANEDIOL (UNII: RUN0H01QEU)  
    CHAMOMILE (UNII: FGL3685T2X)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10742-8451-1295 mL in 1 BOTTLE; 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(10742-8451)
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