Label: HAND ANTIBACTERIAL WIPES- benzalkonium chloride cloth

  • NDC Code(s): 79530-003-01, 79530-003-02
  • Packager: Namco Manufacturing INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 21, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient(s)

    Benzalkonium Chloride 0.13%

  • Purpose

    Antimicrobial Agent

  • Use

    Decreases bacteria on skin.

  • Warnings

    For external use only.

  • Do not use

    Do not use if you are allergic to any of the ingredients.

  • WHEN USING

    Using this product do not get into eyes. lf contact occurs, rinse thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if irritation or rash develops and continues for 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.

  • Directions

    Tear open dispensing cap and remove entire lid from canister.

    Locate wipe at center of the roll,twist corner to a point and thread through small opening in lid.

    Replace lid and pull wipe up at an angle.Remaining wipes feed automatically.

    Snap lid cap shut to retain moisture when finished.

  • Inactive ingredients

    C12-14 Alkyl Dimethyl, Ethylbenzyl Ammonium Chloride, Alkyl Polyglucoside, Disodium EDTA, Propylene Glycol, Aqua.

  • Package Label - Principal Display Panel

    NDC:79530-003-01 Namco Hand Antibacterial wipes 800pcs

    NDC:79530-003-02

    label-80 wipes

  • INGREDIENTS AND APPEARANCE
    HAND ANTIBACTERIAL WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79530-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) (UNII: G258TFN61X)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79530-003-013360 g in 1 PAIL; Type 0: Not a Combination Product07/11/2020
    2NDC:79530-003-02270 g in 1 PAIL; Type 0: Not a Combination Product08/27/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/11/2020
    Labeler - Namco Manufacturing INC. (058595448)
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