Label: AVANCE INCONTINENCE CARE- benzethonium chloride solution

  • NDC Code(s): 70936-112-08
  • 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% (W/W)

  • PURPOSE

    ANTISEPTIC

  • USES

    • PREVENTS SKIN INFECTION
    • KILLS GERMS
  • WARNINGS

    • FOR EXTERNAL ONLY

    DO NOT USE:

    • ON WILD OR DOMESTIC ANIMAL BITES. IF YOU HAVE AN ANIMAL BITE, CONSULT YOUR PHYSICIAN IMMEDIATELY.
    • ON INFECTIONS
    • FOR MORE THAN 10 DAYS. IF INFECTION WORSENS OR PERSISTS, SEE YOUR PHYSICIAN.

    WHEN USING THIS PRODUCT:

    • AVOID CONTACT WITH EYES
  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDERN. IF SWALLOWED GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY

  • DIRECTIONS

    • Apply to affected area
    • Spray on a clean cloth and remove urine, feces and vomit.
    • Cleanse skin of all residue and wipe with clean cloth to dry. If the surface area is massive, rinse affected area with warm water before using.

  • OTHER INFORMATION

    • STORE AT ROOM TEMPERATURE
    • USE ON INFANTS, CHILDREN OR ADULTS
  • INACTIVE INGREDIENTS

    Water, Polysorbate 60, Sodium Methyl Cocoyl Taurate, Cocamidopropyl Betaine, Aloe Barbadensis Leaf Juice, Zinc PCA, Allantoin, Panthenol, Glycerin, Butylene Glycol, PEG-12 Dimethicone, Citric Acid, Ethylhexylglycerin, Fragrance, Phenoxyethanol, Potassium Sorbate.

  • QUESTIONS?

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

  • PRINCIPAL DISPLAY PANEL

    01b LBL (bottle)_Avance_Antibacterial Skin Wash_BZC

  • INGREDIENTS AND APPEARANCE
    AVANCE INCONTINENCE CARE 
    benzethonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70936-112
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.12 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PANTHENOL (UNII: WV9CM0O67Z)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    ZINC PIDOLATE (UNII: C32PQ86DH4)  
    ALLANTOIN (UNII: 344S277G0Z)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PEG-12 DIMETHICONE (UNII: ZEL54N6W95)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70936-112-08237 g in 1 BOTTLE; Type 0: Not a Combination Product06/29/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/29/2022
    Labeler - SMART CHOICE MEDICAL INC. (046383276)
    Registrant - SMART CHOICE MEDICAL INC. (046383276)
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