Label: SALISKIN WASH- salicylic acid gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated October 4, 2019

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  • PRINCIPAL DISPLAY PANEL

    Saliwash

    SALICYLIC ACID, TEA TREE OIL

    CARBOMER, XANTHAM GUM, TRIETHANOLAMINE, ALOE VERA, MINERAL OIL, PROPYLENE GLYCOL, POLYSORBATE 80, PRESERVED WATER, METHYLPARABEN, PROPYLPARABEN, POLYETHYLENE GLYCOL 400

    USE 5-6 PRIOR TO CHEMICAL PEEL.

    DISPENSE A DIME-SIZED AMOUNT AND APPLY TO SKIN.

    SPEND EXTRA TIME ON PROBLEM AREAS

    RINSE USING WARM WATER.

    USE AT LEAST 2-3 TIMES A WEEK FOR 12 WEEKS FOR OPTIMAL RESULTS

    FOR EXTERNAL USE ONLY.

    AVOID CONTACT TO EYES.

    KEEP OUT OF REACH OF CHILDREN.

    STOP USE AND CONSULT DOCTOR IF CONDITION WORSENS OR CLEARS UP AND REOCCURS

    REDUCES PORES

    BLACKHEADS

    REMOVE CYSTIC ACNE

    KEEP OUT OF REACH OF CHILDREN

    REDUCES PORES

    BLACKHEADS

    REMOVE CYSTIC ACNE

  • INGREDIENTS AND APPEARANCE
    SALISKIN WASH 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71718-501
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 2 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER 980 (UNII: 4Q93RCW27E)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ALOE VERA LEAF POLYSACCHARIDES (UNII: W21O437517)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    WATER (UNII: 059QF0KO0R)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71718-501-01113 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product10/04/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/04/2019
    Labeler - Scientific Solutions Global LLC (097291290)
    Registrant - Scientific Solutions Global LLC (097291290)
    Establishment
    NameAddressID/FEIBusiness Operations
    Scientific Solutions Global LLC097291290manufacture(71718-501)
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