Label: ZAPZYT ACNE WASH CLEANSER- salicylic acid gel

  • NDC Code(s): 71687-0007-1
  • Packager: Focus Consumer Healthcare, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 8, 2024

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  • ACTIVE INGREDIENT

    Salicylic Acid 2%

  • PURPOSE

    For the treatment of acne

  • WARNINGS

    For external use only.

    When using this product.

    • avoid contact with eyes. If contact occurs, flush thoroughly with water
    • using other topical acne medications at the same time or immediately following the use of this product may increase dryness or irritation of the skin. If this occurs only one medication should be used unless directed by a physician
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    • use twice daily
    • add water
    • apply to hands
    • massage gently to the affected area
    • rinse thoroughly
  • INDICATIONS & USAGE

    For external use only.

  • Inactive ingredients

    Aloe Barbadensis Leaf Juice, Chamomile Recutita (Matricaria) Flower Extract, Cocamidopropyl Betaine, Disodium EDTA, DMDM Hydantoin, PEG-120 Methyl Glucose Dioliate, Propylene Glycol, Purified Water, Sodium C14-16 Olefin Sulfanate, Sodium Chloride, Sodium Hydroxide

  • PRINCIPAL DISPLAY PANEL

    ZAPZYT

    ACNE WASH CLEANSER

    satisfaction guaranteed

    clinically proven safe and effective on sensitive skin

    dermatologist recommended

    salicylic acid acne medication

    NET WT 6.25 OZ (177g)

    Zapzyt Acne Wash

  • INGREDIENTS AND APPEARANCE
    ZAPZYT ACNE WASH CLEANSER 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71687-0007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    WATER (UNII: 059QF0KO0R)  
    CHAMOMILE (UNII: FGL3685T2X)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71687-0007-1188.5 g in 1 TUBE; Type 0: Not a Combination Product12/16/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00612/16/2017
    Labeler - Focus Consumer Healthcare, LLC (080743737)
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