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PROVON Antibacterial Foam Handwash

Medically reviewed by Drugs.com. Last updated on Nov 9, 2021.

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

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-533
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN0.003 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage Description
1NDC:21749-533-891200 mL in 1 BOTTLE
2NDC:21749-533-901250 mL in 1 BOTTLE
3NDC:21749-533-97700 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/201312/01/2021
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.036424534manufacture(21749-533)

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