Label: ALL CLEAR FACE WASH ACNE CONTROL- salicylic acid paste

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 21, 2021

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  • Drug Facts

  • Active Ingredient

    Salicylic Acid 2%

    Purpose

    Acne medication

  • Use

    For the treatment of acne

  • Warnings

    For external use only.

    When using this product

    • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

    Keep out if reach of children.

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

  • Directions

    • Clean the skin thoroughly before applying this product
    • Cover the entire affected area with a thin layer and rinse thoroughly one to three times daily
    • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
    • If bothersome dryness or peeling occurs, reduce application to once a day or every

  • Inactive Ingredients

    Water (Aqua), sodium hydroxide, pentylene glycol, propanediol, glycolic acid, dimethylisosorbide, gluconolactone, xanthan gum, sodium benzoate

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    ALL CLEAR FACE WASH ACNE CONTROL 
    salicylic acid paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78706-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78706-005-0030 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D01/01/2022
    Labeler - Virgin Scent Inc. (034474058)
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