Label: SMART SAN HAND SANITIZER- ethanol liquid

  • NDC Code(s): 59900-117-02, 59900-117-03, 59900-117-04, 59900-117-05, view more
    59900-117-06, 59900-117-07, 59900-117-08
  • Packager: Best Sanitizers, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 4, 2019

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  • Active Ingredient

    Ethanol 62%

  • Purpose

    Hand Sanitizer

  • Uses

    • Sanitize hands to help reduce bacteria that potentially can cause 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, DEA-C8-18, perfluomalkylethyl phosphate, glycereth-2 cocoate

  • Questions?

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

  • PRINCIPAL DISPLAY PANEL

    NDC 59900--117-02

    NDC 59900--117-03

    NDC 59900--117-04

    NDC 59900--117-05

    NDC 59900--117-06

    NDC 59900--117-07

    NDC 59900--117-08

    Smart San™ Hand Sanitizer Foam

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    SMART SAN HAND SANITIZER 
    ethanol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59900-117
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL620 mL  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE (UNII: 4J55VM509S)  
    GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59900-117-023785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2008
    2NDC:59900-117-03189250 mL in 1 DRUM; Type 0: Not a Combination Product12/01/2008
    3NDC:59900-117-04500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2008
    4NDC:59900-117-051000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2008
    5NDC:59900-117-06118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2008
    6NDC:59900-117-0759 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2008
    7NDC:59900-117-081000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E12/01/2008
    Labeler - Best Sanitizers, Inc (957473614)
    Establishment
    NameAddressID/FEIBusiness Operations
    Best Sanitizers, Inc627278224manufacture(59900-117)
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