PROVON ANTIBACTERIAL PLUM FOAM HANDWASH- triclosan liquid

PROVON Antibacterial Plum Foam Handwash by

Drug Labeling and Warnings

PROVON Antibacterial Plum Foam Handwash 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

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), Alcohol, Lauric Acid, Propylene Glycol, Ethanolamine, Disodium Cocoamphodiacetate, Isopropyl Alcohol, Polyquaternium-10, Prunus Domestica Fruit Extract, Sodium Metabisulfite, Sodium Sulfite, Tetrasodium EDTA, Sodium Sulfate, Fragrance (Parfum), Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PROVON ANTIBACTERIAL PLUM FOAM HANDWASH 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-542
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)
PLUM (UNII: 67M3EQ6BE1)
Sodium Metabisulfite (UNII: 4VON5FNS3C)
Sodium Sulfite (UNII: VTK01UQK3G)
EDETATE SODIUM (UNII: MP1J8420LU)
Sodium Sulfate (UNII: 0YPR65R21J)
Methylchloroisothiazolinone (UNII: DEL7T5QRPN)
Methylisothiazolinone (UNII: 229D0E1QFA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-542-97	700 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2011
2	NDC: 21749-542-89	1200 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2011
3	NDC: 21749-542-90	1250 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/01/2011	12/01/2021

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		036424534	manufacture(21749-542)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		088312414	label(21749-542) , pack(21749-542)