GOJO E2 FOAM SANITIZING SO AP- triclosan liquid

GOJO E2 Foam Sanitizing So ap by

Drug Labeling and Warnings

GOJO E2 Foam Sanitizing So ap by is a Otc medication manufactured, distributed, or labeled by GOJO Industries, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Triclosan 0.3%

Purpose

Antimicrobial

Use

Antiseptic cleanser to help reduce bacteria on skin that could cause disease

Recommended for repeated use

Warnings

For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if irritation or rash appears and lasts

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Wet hands
• Apply a small amount of soap and work into a rich lather
• Rinse thoroughly with potable water
• Dry hands completely

Inactive ingredients

Water (Aqua), Alcohol, Lauric Acid, Propylene Glycol, Ethanolamine, Disodium Cocoamphodiacetate, Isopropyl Alcohol, Polyquaternium-10, Sodium Metabisulfite, Sodium Sulfite, Tetrasodium EDTA, Sodium Sulfate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOJO E2 FOAM SANITIZING SO AP 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-543
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)
ALCOHOL (UNII: 3K9958V90M)
LAURIC ACID (UNII: 1160N9NU9U)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
MONOETHANOLAMINE (UNII: 5KV86114PT)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
SODIUM SULFITE (UNII: VTK01UQK3G)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM SULFATE (UNII: 0YPR65R21J)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-543-89	1200 mL in 1 PACKAGE; Type 0: Not a Combination Product	01/01/2012
2	NDC: 21749-543-90	1250 mL in 1 PACKAGE; Type 0: Not a Combination Product	01/01/2012
3	NDC: 21749-543-20	2000 mL in 1 PACKAGE; Type 0: Not a Combination Product	01/01/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/01/2012

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		036424534	manufacture(21749-543)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		088312414	label(21749-543) , pack(21749-543)