Label: BYOMA ACNE CLEARING BODY WASH- salicylic acid liquid

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

Drug Label Information

Updated April 23, 2025

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  • Drug Facts

  • Active ingredient

    Salicylic Acid 2%

  • Purpose

    Acne Treatment

  • 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.
    • rinse right away with water if it gets in eyes.

    Stop use and ask a doctor if

    • skin irritation occurs or gets worse.

    Keep out of reach of children.

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

  • Directions

    • Wet the skin and gently massage for 1-2 minutes and rinse well.
    • If bothersome dryness or peeling occurs, reduce frequency of use.
  • Other Information

    Protect the product in this container from excessive heat and direct sun.

  • Inactive Ingredients

    Aqua (Water), Ammonium Lauryl Sulfate, Hamamelis Virginiana (Witch Hazel) Water, Cocamidopropyl Betaine, Propylene Glycol, Glycerin, Sodium Chloride, Ethyl Linoleate, Benzyl Alcohol, Sodium Hydroxide, Hydroxypropyl Guar Hydroxypropyltrimonium Chloride, Sodium Benzoate, Phytosphingosine, Ceramide NP, Citric Acid, Bakuchiol, Phenoxyethanol, Propanediol, Glucomannan, Xylitylglucoside, Anhydroxylitol, Rutin, Hydroxycinnamic Acid, Xylitol, Rhamnose, Glucuronic Acid, Glucose.

  • Questions or Comments?

    Contact hello@byoma.com

  • Product Labeling

    1

  • INGREDIENTS AND APPEARANCE
    BYOMA ACNE CLEARING BODY WASH 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84821-005
    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
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLUCOSE (UNII: 5SL0G7R0OK)  
    WATER (UNII: 059QF0KO0R)  
    BAKUCHIOL (UNII: OT12HJU3AR)  
    HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
    PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    RHAMNOSE (UNII: QN34XC755A)  
    ETHYL LINOLEATE (UNII: MJ2YTT4J8M)  
    HYDROXYPROPYL GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (UNII: MVW5LK6LFT)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ANHYDROXYLITOL (UNII: 8XWR7NN42F)  
    HYDROXYCINNAMIC ACID (UNII: IBS9D1EU3J)  
    XYLITOL (UNII: VCQ006KQ1E)  
    GLUCURONIC ACID (UNII: 8A5D83Q4RW)  
    RUTIN (UNII: 5G06TVY3R7)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    CERAMIDE NP (UNII: 4370DF050B)  
    GLUCOMANNAN (UNII: 36W3E5TAMG)  
    XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84821-005-01400 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/12/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00605/12/2025
    Labeler - Byoma Ltd (228554984)
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