PROVON FOAMING MEDICATED HANDWASH WITH MOISTURIZERS AND TRICLOSAN- triclosan liquid

PROVON Foaming Medicated Handwash with Moisturizers and Triclosan by

Drug Labeling and Warnings

PROVON Foaming Medicated Handwash with Moisturizers and Triclosan 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

• Handwash to help decrease bacteria on the skin before and after contact with a person under medical care or treatment
• 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 product and work into a lather
• Rinse well and dry hands completely

Inactive ingredients

Water (Aqua), Propylene Glycol, Alcohol, Lauric Acid, Ethanolamine, Disodium Cocoamphodiacetate, Lactic Acid, Isopropyl Alcohol, PEG-4, Polyquaternium-10, Sodium Metabisulfite, Sodium Sulfite, Tetrasodium EDTA, Sodium Sulfate, Fragrance (Parfum), Iodopropynyl Butylcarbamate, Green 3 (CI 42053)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PROVON FOAMING MEDICATED HANDWASH WITH MOISTURIZERS AND TRICLOSAN 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-096
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)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-096-89	1200 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/30/2009
2	NDC: 21749-096-90	1250 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/30/2009
3	NDC: 21749-096-97	700 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/30/2009
4	NDC: 21749-096-53	535 mL in 1 PACKAGE; Type 0: Not a Combination Product	11/30/2009
5	NDC: 21749-096-20	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/30/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/30/2009	12/01/2020

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		036424534	manufacture(21749-096)