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
  • 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 August 20, 2020

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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 not finalpart333E11/12/2012
    Labeler - Betco Corporation, Ltd (024492831)
    Registrant - Betco Corporation, Ltd (024492831)
    Establishment
    NameAddressID/FEIBusiness Operations
    Betco Corporation, Ltd024492831manufacture(65601-759) , label(65601-759)
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