Label: BENZALKONIUM CHLORIDE ANTISEPTIC TOWELETTE- benzalkonium chloride towelette 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 August 31, 2022

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  • Active Ingredient

    Benzalkonium Chloride, 0.13%

    Purpose

    First Aid Antiseptic

  • Uses

    First Aid Antiseptic

  • Warnings

    For External Use Only

    Do Not Use

    For deep puncture wounds, animal bites or serious burns

    In the eyes

    Over large areas of the body

    Stop Use and ask a doctor if

    if irritation and redness develops and persists for more than 72 hours

    Keep out of reach of children

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

  • Directions

    Open packet and use as a washcloth.

    As a first aid antiseptic

    Clean affected area

    Apply 1 to 3 times daily

    May be covered with a sterile bandage

    If bandaged, let dry first

    Other Information

    Store at room temperature

    Avoid excessive heat

  • Inactive Ingredients

    Purified Water

  • GREIGHT Benzalkonium Chloride Towelette - 1pc

    GR8-BCT-001

  • INGREDIENTS AND APPEARANCE
    BENZALKONIUM CHLORIDE ANTISEPTIC TOWELETTE 
    benzalkonium chloride towelette swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72766-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.8 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72766-011-011 in 1 PACKET; Type 0: Not a Combination Product08/31/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/31/2022
    Labeler - Yangzhou Suxiang Medical Instrument Co., Ltd. (543387280)
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