Label: CLEANSOL ANTIBACTERIAL WET WIPES- benzalkonium choloride cloth

  • NDC Code(s): 84247-002-01, 84247-002-02
  • Packager: Oceanline LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 9, 2024

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  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Uses

    To decrease bacteria on skin

  • Warnings

    For external use only

  • When using this product

    When using this product, avoid contacting eyes. In cases of eye contact, rinse eyes thoroughly with water

  • Stop use and ask a doctor

    Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours

  • Keep out of reach of children

    Keep out of reach of children, if swallowed, get medical help or contact a Poison Control Center immediately

  • Directions

    • Remove lid, open cap, thread wipe through slit and close lid
    • Gently remove wipe, clean skin thoroughly, and allow hands to dry
    • Do not flush, dispose in a waste basket, and close lid after use
    • Store at room temperature and protect from sun exposure
    • For children under 2 years old, ask a doctor before use
  • Other Information

    Production date, expiration date, and lot number are printed on the package

  • Inactive Ingredients

    Water, Phenoxyethanol, Peg 7 Glyceryl Cocoate, Polysorbate 20, Glycerin, Perfume (Lime Oil), Cocamidopropyl Betaine, Citric Acid, Limonene, Hexyl Cinnamal, Citral, Citronellol, Geraniol, Benzyl Benzoate, Linalool

  • Package Label - Principal Display Panel

    cleansol antibacterial wet wipes 100 wipes lime scentcleansol antibacterial wet wipes drug facts

  • INGREDIENTS AND APPEARANCE
    CLEANSOL ANTIBACTERIAL WET WIPES 
    benzalkonium choloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84247-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
    WATER (UNII: 059QF0KO0R)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    LIME OIL (UNII: UZH29XGA8G)  
    GERANIOL (UNII: L837108USY)  
    BENZYL BENZOATE (UNII: N863NB338G)  
    CITRAL (UNII: T7EU0O9VPP)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84247-002-01100 in 1 POUCH05/01/2024
    13.24 g in 1 PATCH; Type 0: Not a Combination Product
    2NDC:84247-002-02100 in 1 CANISTER05/01/2024
    23.24 g in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/01/2024
    Labeler - Oceanline LLC (080450983)
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