Label: TAZZA HAND SANITIZER GYM WIPES- benzalkonium chloride cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 10, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Benzalkonium Chloride 0.13%

  • PURPOSE

    Purpose

    Antimicrobial

  • INDICATIONS & USAGE

    Uses

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

    Warnings

    For external use only

  • WHEN USING

    When using this productavoid contact with eyes. In case of contact, flush eyes thoroughly with water.

  • STOP USE

    Stop use and ask a doctor ifirritation 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

    • take wipe and rub thoroughly over all surfaces of both hands
    • rub hands together briskly to dry
    • dispose of wipe in trash; do not flush
  • INACTIVE INGREDIENT

    Inactive ingredientsWater, Ethyl Alcohol, Acetic Acid (Vinegar), Cocamidopropyl Betaine, Decyl Glucoside, Phenoxyethanol, Acrylates Copolymer, Aloe Barbadensis Leaf Extract,

  • SPL UNCLASSIFIED SECTION

    Made in China

    Manufactured for

    Tazza Brands East

    4140 Mound Road

    Joliet, IL 60436

  • PRINCIPAL DISPLAY PANEL

    1500 Wet Wipes / XL SIZE

    7in x 5in (17.7cm x 12.7cm)
    NDC: 76370-0017-0

    Label 1

    Label 2

  • INGREDIENTS AND APPEARANCE
    TAZZA HAND SANITIZER  GYM WIPES
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76370-0017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ACETIC ACID (UNII: Q40Q9N063P)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76370-0017-01500 in 1 BAG06/10/2022
    11.1 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)06/10/2022
    Labeler - Tazza Brands East Inc (117842371)
    Registrant - Tazza Brands East Inc (117842371)
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