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

  • NDC Code(s): 70924-002-01, 70924-002-02, 70924-002-03, 70924-002-04, view more
    70924-002-05, 70924-002-06, 70924-002-07, 70924-002-09, 70924-002-10, 70924-002-11, 70924-002-12, 70924-002-13, 70924-002-14, 70924-002-15, 70924-002-16, 70924-002-17
  • 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 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.
    • Children under 6 years of age should be supervised when using this product.
    • Be sure to use entire wipe.
    • Discard after single use.
  • Inactive ingredients

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

  • 1500 Wipe Pouch Label

    Touch

    Point™

    Sanitizing Wipes

    1500 Wipes • 8"x 6"

    Fragrance Free

    Kills 99.99%

    of most common germs that may cause illness

    PRINCIPAL DISPLAY PANEL - 1500 Wipe Pouch Label

  • INGREDIENTS AND APPEARANCE
    TOUCHPOINT WIPES FRAGRANCE FREE  SANITIZING WIPES
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70924-002
    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
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
    POLY(LAURYLGLUCOSIDE)-7 (UNII: VB00RDE21R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70924-002-022 in 1 BOX09/09/2016
    1NDC:70924-002-011500 in 1 POUCH; Type 0: Not a Combination Product
    2NDC:70924-002-042 in 1 BOX12/11/2018
    2NDC:70924-002-031800 in 1 POUCH; Type 0: Not a Combination Product
    3NDC:70924-002-062 in 1 BOX12/11/2018
    3NDC:70924-002-052400 in 1 POUCH; Type 0: Not a Combination Product
    4NDC:70924-002-092 in 1 BOX12/11/2018
    4NDC:70924-002-07400 in 1 POUCH; Type 0: Not a Combination Product
    5NDC:70924-002-116 in 1 BOX12/11/2018
    5NDC:70924-002-10320 in 1 CANISTER; Type 0: Not a Combination Product
    6NDC:70924-002-136 in 1 BOX10/16/2019
    6NDC:70924-002-12150 in 1 CANISTER; Type 0: Not a Combination Product
    7NDC:70924-002-152 in 1 BOX11/11/2019
    7NDC:70924-002-142200 in 1 POUCH; Type 0: Not a Combination Product
    8NDC:70924-002-172 in 1 BOX09/21/2022
    8NDC:70924-002-16650 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)09/09/2016
    Labeler - Innocore Sales & Marketing Inc (201152597)
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