Label: ALCOHOL FREE FOAMING HAND SANITIZER- benzalkonium chloride soap

  • NDC Code(s): 65601-700-03, 65601-700-04, 65601-700-05, 65601-700-29, view more
    65601-700-53, 65601-700-55, 65601-700-57, 65601-700-88
  • Packager: Betco Corporation, Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 3, 2024

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  • Alcohol Free Foaming Hand Sanitizer

    ​Active Ingredient

    Benzalkonium Chloride 0.13%

  • Alcohol Free Foaming Hand Sanitizer

    Uses

    • Hand sanitizer to remove microorganisms on the skin.
    • Use this product when soap and water are not available.
  • Alcohol Free Foaming Hand Sanitizer

    Warnings

    • For external use only.
    • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
    • Discontinue use is irritation or redness develops.
    • If irritation persists for more than 72 hours, consult a physician.
    • KEEP OUT OF REACH OF CHILDREN.
    • If swallowed, get medical help or contact a Poison Control Center right away.
  • Alcohol Free Foaming Hand Sanitizer

    Directions

    • ​Read the entire label before using this product.
    • ​Dispense 2 pumps of product onto palm of hand and rub thoroughly over all surfaces of both hands until dry.
  • Alcohol Free Foaming Hand Sanitizer

    Inactive Ingredients

    Deionized ​Water, Sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone,  PEG-3 Cocamide, Fragrance, Methyl Chloro Isothiazolinone, Methyl Isothiazolinone,  D&C Green #5.

  • Alcohol Free Foaming Hand Sanitizer

    Questions or Comments?Phone: (800) 777-9343

    MDS information:​(800) 891-4965

  • Alcohol Free Foaming Hand Sanitizer

    Purpose

    Antiseptic

  • Alcohol Free Foaming Hand Sanitizer

    KEEP OUT OF REACH OF CHILDREN

  • Alcohol Free Foaming Hand Sanitizer

    5329880455

  • INGREDIENTS AND APPEARANCE
    ALCOHOL FREE FOAMING HAND SANITIZER 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65601-700
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GRAPEFRUIT OIL (UNII: YR377U58W9)  
    BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    CYCLOMETHICONE 4 (UNII: CZ227117JE)  
    ACETALDEHYDE (UNII: GO1N1ZPR3B)  
    GERANIOL (UNII: L837108USY)  
    HEXAMETHYLINDANOPYRAN (UNII: 14170060AT)  
    DIHYDROMYRCENOL (UNII: 46L1B02ND9)  
    METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)  
    MYRCENE (UNII: 3M39CZS25B)  
    SODIUM PIDOLATE (UNII: 1V74VH163T)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) (UNII: 9U1Q4T4ZYS)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    ORANGE OIL (UNII: AKN3KSD11B)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    PEG/PPG-15/15 ALLYL ETHER ACETATE (UNII: 8RP39FN7AJ)  
    HEXYL SALICYLATE (UNII: 8F78EY72YL)  
    ALCOHOL (UNII: 3K9958V90M)  
    LIME OIL (UNII: UZH29XGA8G)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    WATER (UNII: 059QF0KO0R)  
    DIOXANE (UNII: J8A3S10O7S)  
    PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)  
    LEMON OIL (UNII: I9GRO824LL)  
    Product Characteristics
    ColorblueScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65601-700-5350 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/01/2016
    2NDC:65601-700-291000 mL in 1 BAG; Type 0: Not a Combination Product01/01/2016
    3NDC:65601-700-043780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2016
    4NDC:65601-700-57550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/01/201609/11/2020
    5NDC:65601-700-55207900 mL in 1 DRUM; Type 0: Not a Combination Product01/01/2016
    6NDC:65601-700-03750 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/15/201607/15/2020
    7NDC:65601-700-051250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/15/201609/11/2020
    8NDC:65601-700-88500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/12/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/12/2012
    Labeler - Betco Corporation, Ltd. (005050158)
    Registrant - Betco corporation, Ltd. (005050158)
    Establishment
    NameAddressID/FEIBusiness Operations
    Betco Corporation, Ltd.005050158manufacture(65601-700) , label(65601-700)
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