Label: SALICYLIC FOAM CLEANSER 20% 7.5 OZ solution

  • NDC Code(s): 84785-0028-1
  • Packager: Gazebo Wellness SKIN LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 16, 2024

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  • DOSAGE & ADMINISTRATION

    Skin Beauty Solutions Salicylic Foam, Removes dirt, dead skin, and oil from pores that can cause active acne.

  • WARNINGS

    Directions: Apply cleanser onto wet face and neck, massage and rinse with cool water, Use 3-5 times a week.

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Aqua (Water), Decyl Glucoside, Cocamidopropyl Betaine, Kosher Vegetable Glycerin, Phenoxyethanol, Xanthan Gum (Polysaccharide Gum), Tetrasodium EDTA, d-Calcium Pantothenate (Pro-Vitamin B5).

  • INDICATIONS & USAGE

    Directions: Apply cleanser onto wet face and neck, massage and rinse with cool water, Use 3-5 times a week.

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • PURPOSE

    SKINBEAUTY
    SOLUTIONS-
    Salicylic Foam Cleanser
    20%
    Removes dirt, dead skin, and oil from pores.

    Distributed By: Skin Beauty Solutions Woodbury MN 55129
    7.5oz/225 ml
    MADE INUSA 12M

  • ACTIVE INGREDIENT

    Active Ingredient:

    Salicylic Acid.

  • PRINCIPAL DISPLAY PANEL

    Content of Labeling

    Content of labeling 225 ml

  • INGREDIENTS AND APPEARANCE
    SALICYLIC FOAM CLEANSER 20% 7.5 OZ 
    salicylic foam cleanser 20% 7.5 oz solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84785-0028
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID22.5 mg  in 225 mL
    Inactive Ingredients
    Ingredient NameStrength
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CALCIUM PANTOTHENATE (UNII: 568ET80C3D)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    AQUA (UNII: 059QF0KO0R)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    TETRASODIUM EDTA (UNII: MP1J8420LU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84785-0028-1225 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01610/01/2024
    Labeler - Gazebo Wellness SKIN LLC (119609953)
    Registrant - Gazebo Wellness SKIN LLC (119609953)
    Establishment
    NameAddressID/FEIBusiness Operations
    Gazebo Wellness SKIN LLC119609953manufacture(84785-0028)
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