Label: FRAGRANCE FREE SANITIZING WIPES- benzalkonium chloride cloth

  • NDC Code(s): 71745-001-01, 71745-001-02
  • Packager: GoodEarth Distribution Llc
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 11, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Benzalkonium Chloride 0.13 %

  • Purpose

    Antimicrobal

  • Use

    Hand sanitizer to help reduce bacteria on the skin.

    Recommended for repeated use.

  • Warnings

    For external use only.

    When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly in water.

    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.

  • 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 ingredients

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

  • 1800 Wipe Pouch Label

    GoodEarth

    DISTRIBUTION

    FRAGRANCE FREE

    Kills 99.99%

    of most common germs

    that may cause illness

    Sanitizing

    wipes

    1800

    count

    Premium fabric quickly

    removes dirt and soil

    MICRODOT ∙

    Principal Display Panel - 1800 Wipe Pouch Label

  • INGREDIENTS AND APPEARANCE
    FRAGRANCE FREE SANITIZING WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71745-001
    Route of AdministrationCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg
    Inactive Ingredients
    Ingredient NameStrength
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
    POLY(LAURYLGLUCOSIDE)-7 (UNII: VB00RDE21R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71745-001-022 in 1 BOX09/25/2017
    1NDC:71745-001-011800 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/25/2017
    Labeler - GoodEarth Distribution Llc (079808558)
    Registrant - Innocore Sales & Marketing Inc (201152597)
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