Label: ANTIBACTERIAL WET WIPES- benzalkonium chloride swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated June 28, 2020

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  • Active ingredient

    benzalkonium chloride 0.13%

  • Purpose

    Antibacterial

  • Uses

    for hand sanitizing to decrease bacteria on the skin

    recommended for repeated use

  • Warnings

    For External use only.

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

    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 or redness develop .

  • 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

    take wipe and rub thoroughly over all surfaces ofboth hands
    ·rub hands together briskly to dry·dispose of wipe

  • INACTIVE INGREDIENT

    WATER PROPYLENE GLYCOL OCTHILINONE .ALPHA.-TOCOPHEROL

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL WET WIPES 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73326-002
    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
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GOSSYPIUM BARBADENSE LEAF (UNII: 251DUP3OSN)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73326-002-0148 in 1 CARTON09/13/2019
    130 in 1 BAG
    13 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/13/2019
    Labeler - Jacent Strategic Merchandising, LLC. (081310578)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Qimei Commodity Co.,Ltd.544331136manufacture(73326-002)
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