SKIN CLEANSER- chloroxylenol soap 
Betco Corporation, Ltd.

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Medicated Lotion Skin Cleanser

Medicated Lotion Skin Cleanser

​Active Ingredient

​Chloroxylenol 0.5%

Knuckle Under Medicated

Uses

  • ​For use in a variety of industrial setting including manufacturing, machine shops, maintenance areas and automotive shops.

Knuckle Under Medicated

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.

Knuckle Under Medicated

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.

Knuckle Under Medicated

Inactive Ingredients

​Water, sodium tallate, Sodium Laureth Sulfate, Triisopropanolamine, Alcohol, Tetrasodium EDTA, Sodium Chloride, Coco MIPA, Fragrance,  Cocamidopropropyl Betaine, Glycerin, Methyl Chlorosiothiazolinone, D&C Green #5, FD&C Yellow #5.

Knuckle Under Medicated

Purpose

Antibacterial

Knuckle Under Medicated

KEEP OUT OF REACH OF CHILDREN

Medicated Lotion Skin Cleanser

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SKIN CLEANSER 
chloroxylenol soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65601-865
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM ALUMINIUM SILICATE (UNII: 058TS43PSM)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
TRISODIUM NITRILOTRIACETATE (UNII: E3C8R2M0XD)  
METHYL ALCOHOL (UNII: Y4S76JWI15)  
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
EDETATE SODIUM (UNII: MP1J8420LU)  
TALL OIL ACID (UNII: H9HR63474M)  
ALCOHOL (UNII: 3K9958V90M)  
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
DIISOPROPANOLAMINE (UNII: 0W44HYL8T5)  
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
CALCIUM SILICATE (UNII: S4255P4G5M)  
FORMALDEHYDE (UNII: 1HG84L3525)  
DIOXANE (UNII: J8A3S10O7S)  
SODIUM FERROCYANIDE (UNII: 5HT6X21AID)  
SODIUM CARBONATE (UNII: 45P3261C7T)  
SODIUM GLYCOLATE (UNII: B75E535IMI)  
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65601-865-043780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2016
2NDC:65601-865-063780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/12/2012
3NDC:65601-865-55208000 mL in 1 DRUM; 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)11/12/201207/01/2024
Labeler - Betco Corporation, Ltd. (005050158)
Registrant - Betco corporation, Ltd. (005050158)
Establishment
NameAddressID/FEIBusiness Operations
Betco Corporation, Ltd.005050158manufacture(65601-865) , label(65601-865) , pack(65601-865)

Revised: 7/2024
 
Betco Corporation, Ltd.