Label: ULTRA BLUE ANTIBACTERIAL FOAMING SKIN CLEANSER- benzalkonium chloride soap

  • NDC Code(s): 65601-759-03, 65601-759-04, 65601-759-29, 65601-759-57, view more
    65601-759-88
  • Packager: Betco Corporation, Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 3, 2024

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  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Warnings

    • For external use only. Do not ingest.
    • Avoid contact with eyes.  If contact occurs, rinse thoroughly with water.
    • Stop use and ask a doctor if irritation and redness develop.
    • 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.
  • Directions

    • ?Read the entire label before using this product.
    • ?Dispense 2 pumps of product onto palm of hand and scrub thoroughly over all surfaces of both hands.
    • Rinse with clean water.
  • Inactive Ingredients

    Water, Phenoxyethanol, Cocamine Oxide, Propylene Glycol, Decyl Glucoside, PEG-4 Rapeseedamide, Cocamidopropyl Hydroxysultaine, Glycerin, Fragrance, Sodium Chloride, Tetrasodium EDTA, Citric Acid, Ethanol, Iodopropynyl Butylcarbamate, Benzyl Acetate, Sodium Glycolate, Sodium Hydroxide, Trisodium Nitrilotriacetate, Diethyl Phthalate, FD&C Blue #1.

  • QUESTIONS

    Questions? 888-GO BETCO (888-462-3826)

  • Clario Ultra Blue Antibacterial Foaming Skin Cleanser

    Purpose

    Antibacterial

  • Clario Ultra Blue Antibacterial Foaming Skin Cleanser

    KEEP OUT OF REACH OF CHILDREN

  • Clario Ultra Blue Antibacterial Foaming Skin Cleanser

    Bag 1000 ml

    bag-1000ml

  • INGREDIENTS AND APPEARANCE
    ULTRA BLUE ANTIBACTERIAL FOAMING SKIN CLEANSER 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65601-759
    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
    WATER (UNII: 059QF0KO0R)  
    COCAMINE OXIDE (UNII: QWA2IZI6FI)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PEG-4 RAPESEEDAMIDE (UNII: 89575CN928)  
    COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    ALCOHOL (UNII: 3K9958V90M)  
    BENZYL ACETATE (UNII: 0ECG3V79ZJ)  
    SODIUM GLYCOLATE (UNII: B75E535IMI)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    TRISODIUM NITRILOTRIACETATE (UNII: E3C8R2M0XD)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) (UNII: 9U1Q4T4ZYS)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    2,4-DIMETHYL-3-CYCLOHEXENE CARBOXALDEHYDE (UNII: 452GFV2AFS)  
    METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)  
    CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    GERANIOL (UNII: L837108USY)  
    LIME OIL (UNII: UZH29XGA8G)  
    2-METHYLUNDECANAL (UNII: S94QNS2VY5)  
    .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)  
    ALLYL CYCLOHEXANEPROPIONATE (UNII: H4W9H3L241)  
    GERANYL ACETATE (UNII: 3W81YG7P9R)  
    CITRONELLYL ACETATE (UNII: IZ420RT3OY)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    CITRAL (UNII: T7EU0O9VPP)  
    FORMALDEHYDE (UNII: 1HG84L3525)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65601-759-291000 mL in 1 BAG; Type 0: Not a Combination Product11/12/2012
    2NDC:65601-759-57550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/12/2012
    3NDC:65601-759-03750 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/12/2012
    4NDC:65601-759-043780 mL in 1 BOTTLE; Type 0: Not a Combination Product11/12/2012
    5NDC:65601-759-88500 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, Ltd005050158manufacture(65601-759) , label(65601-759)
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