Label: GENUINE HAND SANITIZER- alcohol gel

  • 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 December 5, 2019

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  • Active Ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antimicrobial

  • Uses

    For handwashing to decrease bacteria on the skin.

  • Warnings

    For external use only.

    Flammable

    Do not use

    in the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and consult a doctor


    if irritation and redness develop and persist for more than 72 hours

  • Directions

    Empty contents into palm. Rub hands until gel dissipates. Recommended for repeated use.

  • Inactive Ingredients

    Propylene glycol, carbomer, titanium dioxide, purified water

  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • PRINCIPAL DISPLAY PANEL

    Genuine Hand Sanitizer

    Instant Gel

    Antiseptic Handwash

    with Vitamin E and Aloe

    Kills 99.9 percent of germs

    Without Water

    Active Ingredient:

    Ethyl Alcohol 62 percent

    Net Wt 0.9g (1/32 oz)

    Manufactured in China For

    Genuine First Aid.

  • PRINCIPAL DISPLAY PANEL


    Genuine Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    GENUINE HAND SANITIZER  
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52124-0006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52124-0006-10.9 g in 1 PACKET; Type 0: Not a Combination Product04/23/2010
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/23/2010
    Labeler - Genuine First Aid LLC (619609857)
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