Label: AVANCE CURE ANTI-BACTERIAL PERINEAL- benzalkonium chloride spray

  • NDC Code(s): 70936-107-11, 70936-107-12, 70936-107-13, 70936-107-14
  • 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:

    • BENZALKONIUM CHLORIDE              0.3%
  • PURPOSE:

    ANTIBACTERIAL

  • USES

    INCONTINENT/OSTOMY CLEANSER, FORMULATED TO COOL AND SOOTHE SKIN, AVENCE CURE ANTI-BACTERIAL PERINEAL SPRAY REDUCES THE RISK OF SKIN IRRITATIONS AND RASHES. AVANCE CURE ANTI-BACTERIAL PERINEAL SPRAY GENTLY HELPS CLEANSE SKIN OF BODILY WASTES, AND PROTECTS AGAINST HARMFUL BACTERIA.

  • WARNINGS:

    • FOR EXTERNAL ONLY

  • 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:

    PERINEAL AREA: SPRAY ONTO THE AREA TO BE CLEANED. GENTLY REMOVE ANY RESIDUE AND WIPE CLEAN WITH MOIST CLOTH. REPEAT AS NEEDED.

  • INACTIVE INGREDIENTS:

    DISODIUM LAURETH SULFOSUCCINATE

    COCAMIDOPROPYL BETAINE

    GLYCERIN

    ALOE BARBADENSIS (ALOE) LEAF JUICE

    PHENOXYETHANOL

    ETHYLHEXYLGLYCERIN

    FRAGRANCE

  • PRINCIPAL DISPLAY PANEL

    AvanceCureAntibacterialSpray

  • INGREDIENTS AND APPEARANCE
    AVANCE CURE ANTI-BACTERIAL PERINEAL 
    benzalkonium chloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70936-107
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70936-107-11120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/22/2016
    2NDC:70936-107-12240 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/22/2016
    3NDC:70936-107-13480 mL in 1 BOTTLE; Type 0: Not a Combination Product08/22/2016
    4NDC:70936-107-14960 mL in 1 BOTTLE; Type 0: Not a Combination Product06/30/2017
    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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