Label: SMART SAN ALCOHOL FREE HAND SANITIZER FOAM- benzalkonium chloride liquid

  • NDC Code(s): 59900-118-06, 59900-118-12, 59900-118-48
  • Packager: Best Sanitizers, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 5, 2024

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  • Active Ingredient

    Benzalkonium Chloride 0.1%

  • Purpose

    Hand Sanitizer

  • Uses

    • Sanitize Hands to help reduce bacteria that potentially can causes disease
    • Helps to prevent cross contamination
    • Helps to prevent drying of the skin
    • Recommended for repeated use
  • Warnings

    • For external use only
    • Flammable, keep away from fire or flame
  • When Using this product

    • Do not use in or near eyes
    • Use in a well-ventilated area
    • Discontinue use if irritation and redness develop
  • Keep out of reach of children

    In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

  • Directions

    • Receive a small amount of foam into palm of hand
    • Rub thoroughly over all surfaces of both hands
    • Rub hands together until dry
  • Other information

    Store in a cool dry place below 104° F

  • Inactive ingredients

    purified water, dihydroxypropyl PEG-5, linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide

  • Questions?

    Contact Best SanitizersMon-Fri 9am-4pm PST at 888-225-3267

  • PRINCIPAL DISPLAY PANEL

    NDC 59900-118-06

    NDC 59900-118-12

    NDC 59900-118-48

    Smart San™ alcohol-free hand sanitizer foam

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    SMART SAN ALCOHOL FREE HAND SANITIZER FOAM 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59900-118
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 g  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)  
    WATER (UNII: 059QF0KO0R)  
    DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
    BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
    DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59900-118-061250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/15/2009
    2NDC:59900-118-12250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/15/2009
    3NDC:59900-118-4850 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/15/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/15/2009
    Labeler - Best Sanitizers, Inc (957473614)
    Establishment
    NameAddressID/FEIBusiness Operations
    Best Sanitizers, Inc627278224manufacture(59900-118)
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