Label: WIPE THOSE HANDS- benzalkonium chloride cloth

  • NDC Code(s): 78091-251-03, 78091-251-04
  • Packager: Mighty Good Solutions, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 16, 2024

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  • Drug Facts

  • Active ingredient

    Benzalkonium Chloride 0.13%

    Purpose

    Antiseptic

  • Use

    For hand sanitizing to decrease bacteria on the skin.

  • Warnings

    For external use only.

    When using this product

    avoid contact with the eyes. In case of contact, flush eyes thoroughly with water.

    Stop use and ask a doctor if

    irritation and redness develop and persist.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Take wipe from pouch and rub thoroughly over all surfaces of both hands.
    • Rub hands together briskly to dry.
    • Supervise children under 6 years of age when using this product.
    • Dispose of wipe.
  • Inactive ingredients

    Ethylhexylglycerin, Glycerin, Phenoxyethanol, Propylene Glycol, Purified Water.

  • Questions or comments?

    Call +1 (401) 307-1925

  • 78091-250-04

    Outer LabelInner Label

  • 78091-250-03

    Label

  • INGREDIENTS AND APPEARANCE
    WIPE THOSE HANDS 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78091-251
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78091-251-0410 in 1 POUCH07/15/2023
    11 in 1 PACKET
    14.05 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    2NDC:78091-251-0342 in 1 POUCH07/15/2023
    24.05 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/15/2023
    Labeler - Mighty Good Solutions, LLC (029982731)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hangzhou Suncilia Yuehui Biotechnology Co.,LTD554551359manufacture(78091-251)
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