Label: HAND SANITIZER- alcohol gel

  • NDC Code(s): 66715-7012-8
  • Packager: Lil' Drug Store Products, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 15, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Ethyl alcohol 62% w/w

  • Purpose

    Antiseptic

  • Use

    • for handwashing to decrease bacteria on the skin
  • Warnings

    Flammable, keep away from fire or flame.

    For external use only.

    Do not use

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

    Stop use and ask a doctor if

    • irritation and redness develop and persists for more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • wet hands thoroughly with product
    • briskly rub hands together until dry
    • supervise children in the use of this product
  • Other information

    • store at room temperature 15° to 30°C (59° to 86°F)
    • may discolor certain fabrics
  • Inactive ingredients

    water, carbomer, fragrance, triethanolamine, glycerin, propylene glycol, isopropyl alcohol, isopropyl myristate, tocopheryl acetate, aloe vera extract

  • Questions or comments?

    call toll-free 1-877-507-6516 (M-F 8AM-4:30PM CST)

  • SPL UNCLASSIFIED SECTION

    Distributed by: Lil' Drug Store Products, Inc.
    1201 Continental Place NE, Cedar Rapids, IA 52402

  • PRINCIPAL DISPLAY PANEL - 30 mL Bottle Blister Pack - Card & Bottle Label

    QUALITY

    GUARANTEED [caduceus]

    Hand

    Sanitizer

    Kills more than

    99.99% of Germs*

    *Effective at eliminating more than 99.99% of many common

    harmful germs and bacteria in as little as 15 seconds.

    [Lil' Drug Store logo]

    1 FL OZ

    (30 mL)

    PDP/PackageBottle Label

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-7012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66715-7012-81 in 1 PACKAGE10/01/2009
    130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/01/2009
    Labeler - Lil' Drug Store Products, Inc (093103646)
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