Label: PEARLIZED ANTIBACTERIAL SKIN CLEANSER- chloroxylenol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 6, 2024

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

View All Sections
  • Active Ingredient

    Chloroxylenol 0.40%

  • Uses

    • ​​Antibacterial hand cleaner.
    • Use in daycare, hospitals, nursing homes, physicians offices, dental offices and clinics
  • Warnings

    • For external use only.
    • Avoid contact with eyes.
    • Children under the age of 6 should be supervised by an adult when using this product.
    • 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.
  • 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, Sodium Laureth lSulfate, Cocamidopropyl betadine, Phenoxyethanol, Coco MIPA, Glycol Stearate, DMDM Hydantoin, Propylene Glycol, Sodium Chloride, Fragrance, Glycerin, Ethanol,  D&C Green #5, FD&C Yellow #5.

  • Purpose

    Antibacterial

  • KEEP OUT OF REACH OF CHILDREN

    Winning Hands Antibacterial

    KEEP OUT OF REACH OF CHILDREN

  • SPL UNCLASSIFIED SECTION

    ©2017 Betco Corporation
    400 Van Camp Road Bowling Green, Ohio 43402
    Made In U.S.A. All Rights Reserved.

    888-GO BETCO (888-462-3826) | Betco.com

  • PRINCIPAL DISPLAY PANEL

    141-01

  • INGREDIENTS AND APPEARANCE
    PEARLIZED ANTIBACTERIAL SKIN CLEANSER 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72024-841
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL4 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)  
    .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)  
    3-(3,4-METHYLENEDIOXYPHENYL)-2-METHYLPROPANAL (UNII: L65EG8H6PA)  
    4-ACETOXY-3-PENTYLTETRAHYDROPYRAN (UNII: 30E3255185)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    2-ISOBUTYL-4-METHYLTETRAHYDROPYRAN-4-OL (UNII: VK5ZHH2T3F)  
    BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
    2-TERT-BUTYLCYCLOHEXYL ACETATE (UNII: 364FV60913)  
    HEXYL SALICYLATE (UNII: 8F78EY72YL)  
    .GAMMA.-UNDECALACTONE (UNII: QB1T0AG2YL)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    LAURIC ISOPROPANOLAMIDE (UNII: 82DUX3RRVU)  
    SODIUM CARBONATE (UNII: 45P3261C7T)  
    GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CALCIUM SILICATE (UNII: S4255P4G5M)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)  
    SODIUM ALUMINIUM SILICATE (UNII: 058TS43PSM)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
    BENZYL ACETATE (UNII: 0ECG3V79ZJ)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    1-(2,3,8,8-TETRAMETHYL-1,2,3,4,5,6,7,8-OCTAHYDRONAPHTHALEN-2-YL)ETHANONE (UNII: 1GD7ODM28Y)  
    DIHYDROMYRCENOL (UNII: 46L1B02ND9)  
    HEXAHYDRO-4,7-METHANOINDEN-6-YL PROPIONATE (UNII: S3ASM14UAS)  
    VERDYL ACETATE (UNII: 5232EN3X2F)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72024-841-043780 mL in 1 JUG; 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 - Fastenal (042653634)
    Registrant - Betco corporation, Ltd. (005050158)
    Establishment
    NameAddressID/FEIBusiness Operations
    Betco Corporation, Ltd.005050158label(72024-841) , manufacture(72024-841)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!