Label: LUXURY ANTIBACTERIAL FOAMING HANDSOAP- benzalkonium chloride liquid

  • NDC Code(s): 56131-859-29
  • Packager: RD Food Service DBA Restaurant Depot
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 26, 2024

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

  • DOSAGE & ADMINISTRATION

    Place enough product on your palm and scrub hands thoroughly over both surfaces of both hands. Rinse with clean water

  • INACTIVE INGREDIENT

    Water, Phenoxyethanol, cocamine oxide, caprylyl/capryl glucoside, Porpylene glycol, PEG-4 rapeseedamide,cocamidopropyl hydroxysultaine, glycerin, fragrance, tetrasodium EDTA, Citric Acid, Acid Blue 9

  • INDICATIONS & USAGE

    Antibacterial Hand Cleaner

    Use in daycare centers, hospitals, nursing homes, physicians offices, dental offices and clinics

  • INSTRUCTIONS FOR USE

    Read entire label before using this product

    place enough product on your palm and scrub thoroughly over all surfaces of both hands. Rinse with clean water.

  • ACTIVE INGREDIENT

    Benzalkonium chloride

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

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

  • PURPOSE

    Antibacterial

  • WARNINGS

    For external use only. Do not ingest

    When using this product avoud contact with eyes

    disocntinue use if irritation or redness develops

    I irritation persist for more than 72 hours, consult a physicain

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    LUXURY ANTIBACTERIAL FOAMING HANDSOAP 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56131-859
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) (UNII: 9U1Q4T4ZYS)  
    .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCAMINE OXIDE (UNII: QWA2IZI6FI)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    LIME OIL (UNII: UZH29XGA8G)  
    COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CITRAL (UNII: T7EU0O9VPP)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM GLYCOLATE (UNII: B75E535IMI)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    ALCOHOL (UNII: 3K9958V90M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    LINALOOL (UNII: D81QY6I88E)  
    TRISODIUM NITRILOTRIACETATE (UNII: E3C8R2M0XD)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    PEG-4 RAPESEEDAMIDE (UNII: 89575CN928)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    2,4-DIMETHYL-3-CYCLOHEXENE CARBOXALDEHYDE (UNII: 452GFV2AFS)  
    CAPRYLYL/CAPRYL GLUCOSIDE (UNII: E00JL9G9K0)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    2-METHYLUNDECANAL (UNII: S94QNS2VY5)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    BENZYL ACETATE (UNII: 0ECG3V79ZJ)  
    GERANIOL (UNII: L837108USY)  
    ALLYL CYCLOHEXANEPROPIONATE (UNII: H4W9H3L241)  
    GERANYL ACETATE (UNII: 3W81YG7P9R)  
    CITRONELLYL ACETATE (UNII: IZ420RT3OY)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:56131-859-291000 mL in 1 BAG; Type 0: Not a Combination Product12/26/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/26/2024
    Labeler - RD Food Service DBA Restaurant Depot (878186774)
    Registrant - Betco Corporation (005050158)
    Establishment
    NameAddressID/FEIBusiness Operations
    Betco Corporation005050158manufacture(56131-859) , label(56131-859)