Label: AVANCE CURE FOAMING BODY CLEANSER- benzethonium chloride solution

  • NDC Code(s): 70936-110-11
  • Packager: SMART CHOICE MEDICAL INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 7, 2024

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  • ACTIVE INGREDIENT:

    Benzethonium chloride 0.12%

  • PURPOSE:

    ANTIBACTERIAL

  • USES

    Assists in the odor and skin treatment of incontinent and bedridden patients.
    Provides moisture to prevent skin breakdown, usually caused by sweat and urine acidity.
    Protects the skin from breakdown and dryness.

  • WARNINGS:

    For external use only

    Do not use:
    On Deep Open Wounds
    On Infections
    On Skin Lacerations

    When using this product:
    Avoid contact with eyes

    Stop use and ask a doctor if:
    Condition worsens or does not improve within 7 days

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children:
    If swallowed or ingested, seek medical attention or contact the Poison Control Center immediately.

  • DIRECTIONS:

    Prepare the affected area by gently cleaning the skin surface before use. Apply a proper amount of foam to the cleansing area. Spread across the area by gently applying on the irritated skin. Repeat the process as needed, or daily to ensure constant protection until the skin is healed.

  • QUESTIONS?

    Call 1-800-768-3801 or visit smartchoicemedical.com

  • INACTIVE INGREDIENTS:

    Water, Propylene Glycol, Citric Acid, Fragrance, Aloe barbadensis Leaf Juice, Maltodextrin, Sodium Polyglutamate, 1,3 Butylene glycol, Ethylhexylglycerin, Phenoxyethanol, Decyl Glucoside, DMDM Hydantoin, Disodium Cocoamphodiacetate

  • PRINCIPAL DISPLAY PANEL

    Temp LBL_Foaming Body Cleanser

  • INGREDIENTS AND APPEARANCE
    AVANCE CURE FOAMING BODY CLEANSER 
    benzethonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70936-110
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.12 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    MONOSODIUM DL-GLUTAMATE (UNII: LX3YQ006AP)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70936-110-11240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product07/02/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/22/2016
    Labeler - SMART CHOICE MEDICAL INC. (046383276)
    Registrant - SMART CHOICE MEDICAL INC. (046383276)
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