Label: AMBI EVEN AND CLEAR EXFOLIATING WASH ACNE TREATMENT- salicylic acid gel

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

Drug Label Information

Updated December 27, 2023

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  • Drug Facts

  • Active ingredient

    Salicylic acid 1.5%

    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.

    Keep out of reach of children.

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

    If pregnant or breast-feeding,

    ask a health professional before use

  • Directions

    • use every morning and evening
    • wet area first
    • apply a dime sized amount to palm and create a lather.
    • gently massage over the face and neck
    • rinse well 
    • may also be used on chest and back
    • 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 other day
  • Inactive ingredients

    aqua (deionized water), disodium laureth sulfosuccinate, sodium cocoyl isetionate, cocamidopropyl betaine, sodium cocoyl taurate, polyacrylate-1 crosspolymer, sodium lauroamphoacetate, stearic acid, jojoba esters, salicylic acid, glycol stearate, zinc PCA, myristic acid, aminomethyl propanol avena sativa (oat) protein, sea whip extract, ethyl vanillin, dehydroacetic acid, benzyl alcohol.

  • Other information

    store at 59°-86°F (15°-30°C)

  • Questions or comments

    1-800-946-6354

  • Package Labeling:

    Bottle

  • INGREDIENTS AND APPEARANCE
    AMBI EVEN AND CLEAR EXFOLIATING WASH ACNE TREATMENT 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73453-166
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID15 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
    SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    ZINC PIDOLATE (UNII: C32PQ86DH4)  
    MYRISTIC ACID (UNII: 0I3V7S25AW)  
    OAT (UNII: Z6J799EAJK)  
    PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5)  
    ETHYL VANILLIN (UNII: YC9ST449YJ)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73453-166-05141 g in 1 TUBE; Type 0: Not a Combination Product07/13/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00607/13/2020
    Labeler - AMBI ENTERPRISES, LLC (117015229)
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