Label: VIE NATURELLE ACNE BODY- benzoyl peroxide liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 5, 2023

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  • DRUG FACTS:

  • Active Ingredients:

    Benzoyl Peroxide 2.5%

    Acne Treatment

  • Use For:

    For the treatment of acne. Clears up acne pimples and blemishes, and allows skin to heal. Helps prevent new pimples and blemishes from forming.

  • Warnings:

    • For external use only.
    • Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin.
    • 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 per day.

    Do not use

    for prolonged periods without consulting a doctor.

    Keep out of reach of children.

    If swallowed, contact physician or poison control center immediately. Store at room temperature.

  • Directions:

    Cleanse the skin thoroughly before applying medication. Apply an even layer over affected area. Do not use on broken skin or large parts of the body. *For best results apply one to three times per day.

  • Other Ingredients:

    Aqua (Deionized Water), Ethylhexylglycerin, Eucalyptus Globulus Oil, Hamamelis Virginiana (Witch Hazel) Distillate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer Melaleuca Alternifolia (Tea Tree) Oil, Phenoxyethanol, Polysorbate-20, Salicylic Acid.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    VIE NATURELLE ACNE BODY 
    benzoyl peroxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73350-105
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE25 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    WITCH HAZEL (UNII: 101I4J0U34)  
    MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73350-105-08237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/05/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00608/05/2019
    Labeler - TNT PRO SERIES (080998718)
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