Label: PERSISTENT BODY ACNE WASH 8.5OZ- salicylic acid liquid

  • NDC Code(s): 58503-169-01
  • Packager: China Ningbo Shangge Cosmetics Technology Corp.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 9, 2023

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  • Active ingredient

    Salicylic Acid (1%)

  • Purpose

    Acne treatment

  • Use

    For the treatment of acne.

  • Warnings

    For external use only.

    When using this product

    • Avoid contact with eyes. If contact occurs, immediately fulsh with water.
    • Skin irritation and dryness is more likely to occur if you use another topical ance medication at the same time. If irritation occurs, only use one topical acne medication at a time.

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Wet body
    • Gently massage over body for 20-30 seconds
    • Rinse thoroughly and pat dry
    • Recommended for daily use
  • Other information

    Store at room temperature

  • Inactive ingredients

    Water

    Sodium C14-16 Olefin Sulfonate

    Cocamidopropyl Hydroxysultaine

    Sorbitol

    Gluconolactone

    Chlorphenesin

    Sodium Hydroxide

    Acrylates Copolymer

    Disodium EDTA

    Glycolic Acid

  • label

    label

  • INGREDIENTS AND APPEARANCE
    PERSISTENT BODY ACNE WASH 8.5OZ 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58503-169
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID1 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    SORBITOL (UNII: 506T60A25R)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
    BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58503-169-01250 mL in 1 BOTTLE; Type 0: Not a Combination Product10/09/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00610/09/2023
    Labeler - China Ningbo Shangge Cosmetics Technology Corp. (529287434)
    Establishment
    NameAddressID/FEIBusiness Operations
    China Ningbo Shangge Cosmetics Technology Corp.529287434manufacture(58503-169)
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