Label: WET ONES- benzethonium chloride swab

  • 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
  • Packager: Energizer Personal Care LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 12/12

If you are a consumer or patient please visit this version.

  • Active Ingredients

    Benzethonium Chloride 0.3%

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  • Purpose

    Antibacterial

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  • Use

    decrease bacteria on skin

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  • Warnings

    For external use only

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  • Do not use

    if you are allergic to any of the ingredients

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  • When using this product

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

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  • Stop use and ask a doctor

    if irritation or rash develops and continues for more than 72 hours

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  • Keep out of reach of children.

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

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  • Directions

    adults and children 2 years and over

    • apply to hands
    • allow to dry without wiping

    Children under 2 years

    • ask a doctor before use
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  • Inactive Ingredients

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

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  • Questions or Comments?

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

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  • Principle Display Panel

    FRESH SCENT

    WET ONES

    ANTIBACTERIAL

    HAND WIPES

    Kills 99.99% of Germs

    cleans better than hand sanitizers

    hypoallergenic

    35 wipes

    Wet Ones Fresh Scent 35 canister

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  • INGREDIENTS AND APPEARANCE
    WET ONES 
    benzethonium chloride swab
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:63354-998
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZETHONIUM CHLORIDE (BENZETHONIUM) BENZETHONIUM CHLORIDE 0.3   in 100 
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    ALCOHOL  
    PEG-8 DIMETHICONE  
    QUATERNIUM-52  
    SODIUM CAPRYLOAMPHOPROPIONATE  
    CITRIC ACID MONOHYDRATE  
    EDETATE DISODIUM  
    ALOE VERA LEAF  
    PHENOXYETHANOL  
    POTASSIUM SORBATE  
    METHYLPARABEN  
    ETHYLPARABEN  
    PROPYLPARABEN  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:63354-998-15 15 in 1 POUCH
    2 NDC:63354-998-20 20 in 1 POUCH
    3 NDC:63354-998-24 24 in 1 PACKAGE
    4 NDC:63354-998-26 26 in 1 PACKAGE
    5 NDC:63354-998-28 28 in 1 POUCH
    6 NDC:63354-998-35 35 in 1 POUCH
    7 NDC:63354-998-36 35 in 1 CANISTER
    8 NDC:63354-998-40 40 in 1 CANISTER
    9 NDC:63354-998-42 42 in 1 CANISTER
    10 NDC:63354-998-48 48 in 1 CANISTER
    11 NDC:63354-998-14 144 in 1 PACKAGE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 10/01/2007
    Labeler - Energizer Personal Care LLC (021718141)
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