Label: WET ONES ANTIBACTERIAL HAND WIPES - EUCALYPTUS AND MINT- benzalkonium chloride swab

  • NDC Code(s): 63354-547-15
  • Packager: Edgewell Personal Care Brands LLC
  • 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 December 13, 2022

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  • Active Ingredient

    Benzalkonium Chloride 0.11%

  • Purpose

    Antimicrobial Agent

  • Use

    decreases bacteria on skin

  • Warnings

    For external use only

    Do not use

    if you are allergic to any of the ingredients

    When using this product

    do not get into eyes. If contact occurs, rinse thoroughly with water.

    Stop use and ask a doctor

    if irritation or rash develops and continues 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

    adults and children 2 years and over - Rub on hands for 30 seconds and allow skin to dry without wiping.

    children under 2 years - ask a doctor before use

  • Inactive Ingredients

    Water, Alcohol Denat., Propylene Glycol, Phenoxyethanol, Caprylyl Glycol, Lauryl Glucoside, Citric Acid, Ethylhexylglycerin, Tetrasodium EDTA, Fragrance, Aloe Barbadensis Leaf Extract, Chamonilla Recutita (Matricaria) Flower Extract.

  • Questions or Comments?

    Call 1-866-WET-111S; (1-866-938-1117), M-F

  • PRINCIPAL DISPLAY PANEL

    WET

    ONES

    ANTIBACTERIAL

    HAND WIPES

    Eucalyptus & Mint

    Kills 99.99% of Germs

    Tough on Germs

    Gentle on Skin

    Hypoallergenic

    Do Not Flush

    150

    wipes

    label

  • INGREDIENTS AND APPEARANCE
    WET ONES ANTIBACTERIAL HAND WIPES - EUCALYPTUS AND MINT 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63354-547
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.11 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    DEHYDRATED ALCOHOL (UNII: 3K9958V90M)  
    CHAMOMILE (UNII: FGL3685T2X)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63354-547-15150 g in 1 CONTAINER; Type 0: Not a Combination Product03/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/01/2023
    Labeler - Edgewell Personal Care Brands LLC (151179769)
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