PROVON Antibacterial Foam Handwash

Dosage form: liquid
Ingredients: TRICLOSAN 0.003mg in 1mL
Labeler: GOJO Industries, Inc.
NDC code: 21749-533

Medically reviewed by Drugs.com. Last updated on Nov 11, 2024.

PROVON Antibacterial Foam Handwash

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, Iodopropynyl Butylcarbamate

PROVON ANTIBACTERIAL FOAM HANDWASH
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21749-533
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (TRICLOSAN)	TRICLOSAN	0.003 mg in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER
PROPYLENE GLYCOL
ALCOHOL
LAURIC ACID
MONOETHANOLAMINE
DISODIUM COCOAMPHODIACETATE
LACTIC ACID
ISOPROPYL ALCOHOL
POLYETHYLENE GLYCOL 200
POLYQUATERNIUM-10 (30000 MPA.S AT 2%)
SODIUM METABISULFITE
SODIUM SULFITE
EDETATE SODIUM
SODIUM SULFATE
IODOPROPYNYL BUTYLCARBAMATE

Packaging
#	Item Code	Package Description
1	NDC:21749-533-89	1200 mL in 1 BOTTLE
2	NDC:21749-533-90	1250 mL in 1 BOTTLE
3	NDC:21749-533-97	700 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/01/2013	12/01/2021

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Operations
GOJO Industries, Inc.		036424534	manufacture(21749-533)

Revised: 11/2018

Document Id: bfffc759-2d42-494a-868e-3154749cdd7e

Set id: db57037d-8827-4438-9729-1c2c49db529c

Version: 2

Effective Time: 20181119

GOJO Industries, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer

Antibiotics 101