Label: WET ONES ANTIBACTERIAL HAND WIPES SPRING BLISS- 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 January 6, 2021

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  • Active Ingredient

    Benzalkonium Chloride 0.11%

  • Purpose

    Antibacterial

  • Use

    to decrease bacteria on skin

  • Warnings

    For external use only

    Do not use

    if you are allergic to any of the ingredients

    if irritation and redness develop

    When using this product

    Keep out of eyes. In case of contact with eyes, flush thoroughly with water,

    Stop use and ask a doctor

    if condition 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

    Adults and children 3 years and over: rub hands thoroughly with product and allow skin to dry without wiping

    Children under 3 years: ask a doctor before use

  • Inactive ingredients

    Water, Ethyl Alcohol, Propylene Glycol, Phenoxyethanol, Lauryl Glucoside, Iodopropynyl Butylcarbamate, Tetrasodium EDTA, 2-Bromo-2-Nitropropane-1,3-Diol, Citric Acid, Fragrance, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract

  • Questions or Comments?

    Call 1-866-WET-111S

    (1-866-936-1117), M-F

  • Primary Display Panel

    ANTIBACTERIAL

    25

    wipes

    63354-904-25

    ANTIBACTERIAL

    Soft Texture

    50

    wipes

    63354-904-50

    Wet

    Ones(r)

    ANTIBACTERIAL

    HAND WIPES

    Spring Bliss

    Touch of Aloe

    Remove Label

    Wet

    Ones(r)

    ANTIBACTERIAL HAND WIPES

    Spring Bliss

    Touch of Aloe

    Top Label

  • INGREDIENTS AND APPEARANCE
    WET ONES ANTIBACTERIAL HAND WIPES SPRING BLISS 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63354-904
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.11 
    Inactive Ingredients
    Ingredient NameStrength
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALCOHOL (UNII: 3K9958V90M)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    BRONOPOL (UNII: 6PU1E16C9W)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    CHAMOMILE (UNII: FGL3685T2X)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63354-904-2525 in 1 POUCH; Type 0: Not a Combination Product01/08/2021
    2NDC:63354-904-5050 in 1 POUCH; Type 0: Not a Combination Product01/08/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/08/2021
    Labeler - Edgewell Personal Care Brands LLC (151179769)
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