Label: GOODEARTH SANITIZING WIPES- benzalkonium chloride cloth

  • NDC Code(s): 71745-003-01
  • Packager: GoodEarth Distribution LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated July 2, 2024

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  • ACTIVE INGREDIENT

    Active Ingredient

    Benzalkonium Chloride 0.13 %

  • PURPOSE

    Purpose

    Antimicrobial

  • INDICATIONS & USAGE

    Use

    Hand sanitizer to help reduce bacteria on the skin.

    Recommended for repeated use.

  • WARNINGS

    Warnings

    For external use only.

  • WHEN USING

    When using this product do not use in or near the eyes.

    In case of contact, rinse eyes thoroughly in water.

  • STOP USE

    Discontinue use if irritation and redness develop.

    If conditions persist for more than 72 hours, consult a physician.

    If swallowed get medical help or contact a poison control

    center immediately.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    Directions

    · Wet hands thoroughly with product and allow to dry.

    · Be sure to use entire wipe.

    · Discard after single use.

    · Children under 6 years of age should be supervised

    when using this product.

  • INACTIVE INGREDIENT

    Inactive Ingredients

    Benzoic Acid, Caprylyl/Capryl Oligoglucoside, Dehydroacetic Acid, Phenoxyethanol, Poly(Laurylglucoside)-7, Propylene Glycol, Water

  • PRINCIPAL DISPLAY PANEL

    3000 Total Wipes (1500 wipes per roll; 2 rolls per case)

    NDC: 71745-003-01

    Product Label - 1500 SHEETS

  • INGREDIENTS AND APPEARANCE
    GOODEARTH SANITIZING WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71745-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE3.822 mg
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    POLY(LAURYLGLUCOSIDE)-7 (UNII: VB00RDE21R)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    WATER (UNII: 059QF0KO0R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71745-003-012 in 1 CASE08/11/2023
    11500 in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/11/2023
    Labeler - GoodEarth Distribution LLC (079808558)
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