Label: WET ONES- benzethonium chloride swab

  • Contains inactivated NDC Code(s)
    NDC Code(s):     63354-998-14, 63354-998-15, 63354-998-20, 63354-998-24, view more
    63354-998-26, 63354-998-28, 63354-998-35, 63354-998-36, 63354-998-40, 63354-998-42, 63354-998-48, 63354-998-65
  • 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 March 1, 2018

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  • Active Ingredient

    Benzethonium Chloride 0.3%

  • Purpose

    Antibacterial

  • Use

    decrease 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

    • apply to hands
    • allow skin to dry without wiping

    children under 2 years

    • ask a doctor before use
  • Inactive Ingredients

    Water, Alcohol Denat., PEG-8 Dimethicone, Phenoxyethanol, Quaternium-52, Potassium Sorbate, Sodium Capryloamphopropionate, Methylparaben, Citric Acid, Disodium EDTA, Fragrance, Ethylparaben, PEG-60 Lanolin, Propylparaben, Aloe Barbadensis Leaf Juice

  • Questions or Comments?

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

  • PDP

    FRESH

    SCENT

    Wet

    Ones

    ANTIBACTERIAL

    HAND WIPES

    Kills 99.99% of Germs

    cleans better than

    hand sanitizers

    hypoallergenic

    6335499840633549984863354998286335499865

  • INGREDIENTS AND APPEARANCE
    WET ONES 
    benzethonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63354-998
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.3   in 100 
    Inactive Ingredients
    Ingredient NameStrength
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM CAPRYLOAMPHOPROPIONATE (UNII: W9H6IT16GQ)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    PEG-60 LANOLIN (UNII: K2OI1D27ET)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALCOHOL (UNII: 3K9958V90M)  
    QUATERNIUM-52 (UNII: 588EQF3H1P)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63354-998-1515 in 1 POUCH; Type 0: Not a Combination Product10/01/200703/01/2018
    2NDC:63354-998-2020 in 1 POUCH; Type 0: Not a Combination Product10/01/2007
    3NDC:63354-998-2424 in 1 PACKAGE; Type 0: Not a Combination Product10/01/2007
    4NDC:63354-998-2626 in 1 PACKAGE; Type 0: Not a Combination Product10/01/200703/01/2018
    5NDC:63354-998-2828 in 1 POUCH; Type 0: Not a Combination Product10/01/2007
    6NDC:63354-998-3535 in 1 POUCH; Type 0: Not a Combination Product10/01/200703/01/2018
    7NDC:63354-998-3635 in 1 CANISTER; Type 0: Not a Combination Product10/01/200703/01/2018
    8NDC:63354-998-4040 in 1 CANISTER; Type 0: Not a Combination Product10/01/2007
    9NDC:63354-998-4242 in 1 CANISTER; Type 0: Not a Combination Product10/01/200703/01/2018
    10NDC:63354-998-4848 in 1 CANISTER; Type 0: Not a Combination Product10/01/2007
    11NDC:63354-998-14144 in 1 PACKAGE; Type 0: Not a Combination Product10/01/2007
    12NDC:63354-998-6565 in 1 CANISTER; Type 0: Not a Combination Product10/01/2007
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A10/01/2007
    Labeler - Edgewell Personal Care Brands LLC (151179769)
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