Label: TOUCHPOINT HAND SANITIZING WIPES FRAGRANCE FREE- benzalkonium chloride cloth

  • NDC Code(s): 70924-003-01, 70924-003-02, 70924-003-03, 70924-003-04
  • Packager: Innocore Sales & Marketing Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

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 productdo not use in or near the eyes. In case of contact, rinse eyes thoroughly in water.

    Discontinue use ifirritation and redness develop. If conditions persist for more than 72 hours, consult a physician.

    If swallowed getmedical 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

  • Questions?

    1.877.910.4809

  • 320 Wipe Canister Label

    Touch
    Point™

    Hand Sanitizing
    Wipes

    FRAGRANCE FREE

    320
    wipes
    (6.6" x 6.75")

    Kills 99.99%
    of most common germs that may cause illness

    PRINCIPAL DISPLAY PANEL - 320 Wipe Canister Label

  • INGREDIENTS AND APPEARANCE
    TOUCHPOINT HAND SANITIZING WIPES FRAGRANCE FREE 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70924-003
    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
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLY(LAURYLGLUCOSIDE)-7 (UNII: VB00RDE21R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70924-003-01320 in 1 CANISTER; Type 0: Not a Combination Product09/24/2020
    2NDC:70924-003-02500 in 1 BAG; Type 0: Not a Combination Product09/24/2020
    3NDC:70924-003-031500 in 1 BAG; Type 0: Not a Combination Product09/24/2020
    4NDC:70924-003-04320 in 1 POUCH; Type 0: Not a Combination Product09/24/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/24/2020
    Labeler - Innocore Sales & Marketing Inc (201152597)
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