Label: SALICYLIC 20 SKIN PEEL solution
SALICYLIC 30 SKIN PEEL- salicylic 20 skin peel solution

  • NDC Code(s): 84785-0013-1, 84785-0013-2, 84785-0013-3, 84785-0013-4, view more
    84785-0013-5, 84785-0013-6, 84785-0014-1, 84785-0014-2, 84785-0014-3, 84785-0014-4, 84785-0014-5, 84785-0014-6
  • Packager: Gazebo Wellness SKIN LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 16, 2024

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  • DOSAGE & ADMINISTRATION

    Note: A stinging sensation may occur. Flakiness may occur for 3-5 days after performing peel. When using this product avoid unnecessary sun exposure and

  • WARNINGS

    DIRECTIONS: Apply the peel to the treatment area. Let stand on skin for 2-10 minutes depending on skin tolerance. Remove peel with copious amount of water. Follow with moisturizer. Note: A stinging sensation may occur. Flakiness may occur for 3-5 days after performing peel. When using this product avoid unnecessary sun exposure and

  • INACTIVE INGREDIENT

    Inactive ingredients: Propylene Glycol, SD Alcohol, Hexylene Glycol.

  • ACTIVE INGREDIENT

    Active ingredient: Salicylic Acid.

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • INDICATIONS & USAGE

    Apply the peel to the treatment area. Let stand on skin for 2-10 minutes depending on skin tolerance. Remove peel with copious amount of water. Follow with moisturizer. Note: A stinging sensation may occur. Flakiness may occur for 3-5 days after performing peel. When using this product avoid unnecessary sun exposure and
    use sunscreen.
    For external use only.

  • PURPOSE

    salicylic acid skin peel
    20%
    Removes Blackheads Cleans Pores
    Clears Acne & Scars

    Distributed By:
    Skin Beauty Solutions Elk Grove CA 95759

  • PRINCIPAL DISPLAY PANEL

    Content of labeing

    Content of labeling 15 mlContent of labeling 30 mlContent of labeling 60 mlContent of labeling 15 mlContent of labeling 30 mlContent of labeling 60 ml

  • INGREDIENTS AND APPEARANCE
    SALICYLIC 20 SKIN PEEL 
    salicylic 20 skin peel solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84785-0013
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.3 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    CITRAL PROPYLENE GLYCOL ACETAL (UNII: 9W7YHX7EX6)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84785-0013-115 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    2NDC:84785-0013-230 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    3NDC:84785-0013-360 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    4NDC:84785-0013-4120 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    5NDC:84785-0013-5240 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    6NDC:84785-0013-6480 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
    SALICYLIC 30 SKIN PEEL 
    salicylic 20 skin peel solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84785-0014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.3 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    CITRAL PROPYLENE GLYCOL ACETAL (UNII: 9W7YHX7EX6)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84785-0014-115 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    2NDC:84785-0014-230 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    3NDC:84785-0014-360 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    4NDC:84785-0014-4120 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    5NDC:84785-0014-5240 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
    6NDC:84785-0014-6480 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(84785-0013, 84785-0014)
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