Label: HAND SANITIZER- ethanol liquid

  • NDC Code(s): 76370-0005-2, 76370-0005-4, 76370-0005-5, 76370-0005-6
  • Packager: Tazza Brands East Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 24, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Ethanol 70%

  • PURPOSE

    Purpose

    Antiseptic

  • INDICATIONS & USAGE

    Uses

    • for hand sanitizing to decrease bacteria on the skin
    • recommended for repeated use
  • WARNINGS

    Warnings

    For external use only

    Flammable. Keep away from fire or flame.

  • WHEN USING

    When using this product avoid contact with eyes. In case of eye contact, flush eyes with water and seek medical help.

  • STOP USE

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

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    Directions

    • apply liberally into palm of hand
    • rub hands together until dry
    • no need to rinse
  • STORAGE AND HANDLING

    Other information

    • do not store above 100°F (38°C)
    • non-staining
    • may discolor some fabrics
  • INACTIVE INGREDIENT

    Inactive ingredients

    Purified Water, Diethanolamine, Propylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice.

  • SPL UNCLASSIFIED SECTION

    Manufactured for Terraboost Media, LLC, 3109 Grand Avenue #300, Miami, FL 33133

    A Product of Terraboost®

    Made in Taiwan [Made in U.S.A.]

    www.tazzabrands.com

  • PRINCIPAL DISPLAY PANEL

    Tazza Instant Hand Sanitizer Foam

    alcohol formula

    Kills 99.99% of Germs

    fragrance free

    6,000 PUMPS

    81.15 Fl.OZ. (2,400mL)

    Tazza ALC TW 112017

    Tazza ALC 112017US

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    ethanol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76370-0005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DIETHANOLAMINE (UNII: AZE05TDV2V)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76370-0005-51000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/17/2017
    2NDC:76370-0005-62400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/17/2017
    3NDC:76370-0005-4946 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/02/2020
    4NDC:76370-0005-23785 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/02/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/17/2017
    Labeler - Tazza Brands East Inc. (117842371)
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