Label: TAZZA HAND SANITIZING FOAM- alcohol liquid

  • NDC Code(s): 76370-0022-1
  • Packager: Tazza Brands East Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 25, 2024

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  • Drug Facts

  • Active ingredient

    Ethanol 63%

  • Purpose

    Antiseptic

  • Uses

    Decreases bacteria on hands

  • Warnings

    Flammable: Keep away from flame or high heat.

    For external use only.

    When using this product keep out of eyes.

    Stop use and ask a doctor if redness or irritation develops.

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

  • Directions

    • Dispense an adequate amount in your palm to cover all surfaces of both hands completely.
    • Rub hands together until dry.
  • Inactive ingredients

    Purified water, glycerin, triethanolamine, carbomer, vitamin E, aloe vera.

  • SPL UNCLASSIFIED SECTION

    Manufactured for Terraboost Media, LLC
    2232 Dell Range Blvd., Suite 202, Cheyenne, WY 82009
    A Product of Terraboost ® • Made in China • www.terraboost.com

  • PRINCIPAL DISPLAY PANEL

    tazza

    HAND SANITIZING FOAM

    63%

    ALCOHOL FORMULA

    1 GALLON (3785 mL)

    Manufactured for Tazza Brands East
    2232 Dell Range Blvd., Suite 202
    Cheyenne, WY 82009
    A Product of Tazza Brands East
    877-837-7210 • www.tazzabrands.biz

    label

  • INGREDIENTS AND APPEARANCE
    TAZZA HAND SANITIZING FOAM 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76370-0022
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL63 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76370-0022-13785 mL in 1 BOTTLE; Type 0: Not a Combination Product01/17/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/17/2024
    Labeler - Tazza Brands East Inc. (117842371)
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