Label: TAZZA-X EXTREME HAND SANITIZING WIPES- ethanol cloth

  • NDC Code(s): 76370-0010-0
  • 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

    Ethyl Alcohol 70%

  • PURPOSE

    Purpose

    Antiseptic

  • INDICATIONS & USAGE

    Uses

    • 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 keep away from eyes. In case of eye contact, rinse eyes with water.

  • STOP USE

    Stop use and ask a doctor if irritation or redness develop or last more than 72 hours

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    Directions

    • rub wipe thoroughly over all surfaces of both hands
    • allow to dry without wiping
    • supervise children under 6 years old
    • not recommended for infants
    • dispose of wipe in trash; do not flush
  • STORAGE AND HANDLING

    Other information

    • store below 100°F (38°C)
  • INACTIVE INGREDIENT

    Inactive ingredients Aloe Barbadensis Leaf Juice, Decyl Glucoside, Glycerin, Propylene Glycol, Purified Water

  • SPL UNCLASSIFIED SECTION

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

    A product of Terraboost® • 877-837-7210 • www.tazzabrands.com • Made in China

  • PRINCIPAL DISPLAY PANEL

    tazza®-X

    EXTREME HAND SANITIZING WIPES

    A product of Terraboost®

    Made with 70% Ethanol Alcohol

    50 Individual Hand Wipes

    6x8 in (15x20 cm) Spunlace

    FRAGRANCE FREE

    76370-0010-0

  • INGREDIENTS AND APPEARANCE
    TAZZA-X EXTREME HAND SANITIZING WIPES 
    ethanol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76370-0010
    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
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76370-0010-050 in 1 CARTON11/27/2020
    11 in 1 POUCH
    13.2 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/27/2020
    Labeler - Tazza Brands East Inc. (117842371)
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