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PROVON Antibacterial Plum Foam Handwash

Medically reviewed on September 15, 2017

Dosage form: liquid
Ingredients: Triclosan 0.003mg in 1mL
Labeler: GOJO Industries, Inc.
NDC Code: 21749-542

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

PROVON Antibacterial Plum Foam Handwash

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)

PROVON ANTIBACTERIAL PLUM FOAM HANDWASH 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-542
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 
Alcohol 
Lauric Acid 
PROPYLENE GLYCOL 
MONOETHANOLAMINE 
Disodium Cocoamphodiacetate 
Isopropyl Alcohol 
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) 
PLUM 
Sodium Metabisulfite 
Sodium Sulfite 
EDETATE SODIUM 
Sodium Sulfate 
Methylchloroisothiazolinone 
Methylisothiazolinone 
FD&C BLUE NO. 1 
D&C RED NO. 33 
Packaging
#Item CodePackage Description
1NDC:21749-542-97700 mL in 1 BOTTLE
2NDC:21749-542-891200 mL in 1 BOTTLE
3NDC:21749-542-901250 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/01/2011
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.036424534manufacture(21749-542)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.088312414label(21749-542), pack(21749-542)

 
GOJO Industries, Inc.

Further information

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

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