KNUCKLE UNDER MEDICATED- chloroxylenol soap

Knuckle Under Medicated by

Drug Labeling and Warnings

Knuckle Under Medicated by is a Otc medication manufactured, distributed, or labeled by Betco Corporation, Ltd., Betco corporation, Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

KNUCKLE UNDER MEDICATED 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65601-765
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
EDETATE SODIUM (UNII: MP1J8420LU)
TALL OIL ACID (UNII: H9HR63474M)
TRIISOPROPANOLAMINE (UNII: W9EN9DLM98)
ALCOHOL (UNII: 3K9958V90M)
TRIMETHYLENEDIAMINETETRAACETIC ACID (UNII: 3F6OA94EER)
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65601-765-19	900 mL in 1 BAG; Type 0: Not a Combination Product	11/12/2012	01/01/2016
2	NDC: 65601-765-10	1100 mL in 1 BAG; Type 0: Not a Combination Product	11/12/2012	01/01/2016
3	NDC: 65601-765-04	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/01/2016
4	NDC: 65601-765-06	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/12/2012
5	NDC: 65601-765-55	208000 mL in 1 DRUM; Type 0: Not a Combination Product	11/12/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/12/2012

Labeler - Betco Corporation, Ltd. (024492831)

Registrant - Betco corporation, Ltd. (024492831)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation, Ltd.		024492831	manufacture(65601-765) , label(65601-765) , pack(65601-765)