GOJO ANTIBACTERIAL FOAM HANDWASH TRICLOSAN LIQUID- triclosan liquid

GOJO Antibacterial Foam Handwash Triclosan Liquid by

Drug Labeling and Warnings

GOJO Antibacterial Foam Handwash Triclosan Liquid by is a Otc medication manufactured, distributed, or labeled by GOJO Industries, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOJO ANTIBACTERIAL FOAM HANDWASH TRICLOSAN LIQUID 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-535
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.003 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALCOHOL (UNII: 3K9958V90M)
LAURIC ACID (UNII: 1160N9NU9U)
MONOETHANOLAMINE (UNII: 5KV86114PT)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
LACTIC ACID (UNII: 33X04XA5AT)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
POLYETHYLENE GLYCOL 200 (UNII: R95B8J264J)
POLYQUATERNIUM-10 (30000 MPA.S AT 2%) (UNII: C7RDC8Y4JS)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
SODIUM SULFITE (UNII: VTK01UQK3G)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM SULFATE (UNII: 0YPR65R21J)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-535-97	700 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/31/2012
2	NDC: 21749-535-89	1200 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/31/2012
3	NDC: 21749-535-90	1250 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/31/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
export only		01/31/2012

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		036424534	manufacture(21749-535)