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Pro Advantage Antibacterial by NDC National Distribution & Contracting, Inc.

Medically reviewed on January 12, 2018

Dosage form: liquid
Ingredients: TRICLOSAN 3mg in 0.001L
Labeler: NDC National Distribution & Contracting, Inc.
NDC Code: 43128-128

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.

Pro Advantage Antibacterial Liquid Soap

Pro Advantage Antibacterial Liquid Soap


Active Ingredient

Triclosan, 0.3%

Purpose

Antiseptic Handwash

Use

Handwash to help reduce bacteria that potentially can cause disease.

Warnings

• For external use only

Ask a doctor before use if you have

• Deep wounds, animals bites, or serious burns.

When using this product

• Avoid contact with eyes. If this occurs, rinse thoroughly with water.

Stop use and ask a doctor if

• Irritation, itching or redness develops. If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children.

• If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Wet hands, apply soap, lather for 30 seconds, and rinse hands thoroughly.

Inactive Ingredients

Water, Sodium Laureth Sulfate, Cocamine Oxide, Sodium Chloride, Cocamidopropyl Betaine, Propylene Glycol, DMDM Hydantoin, Fragrance, FDandC Yellow 5, FDandC Red 40

REF: P778128 NDC 43128-108-03

Made in China
www.ProAdvantagebyNDC.com

Manufactured for NDC, Inc.
407 New Sanford Road, La Vergne, TN 37086

Product Label

PRO ADVANTAGE ANTIBACTERIAL 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43128-128
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN3 mg  in 0.001 L
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURETH-3 SULFATE 
COCAMINE OXIDE 
SODIUM CHLORIDE 
COCAMIDOPROPYL BETAINE 
PROPYLENE GLYCOL 
DMDM HYDANTOIN 
FD&C YELLOW NO. 5 
FD&C RED NO. 40 
Packaging
#Item CodePackage Description
1NDC:43128-128-033.8 L in 1 JUG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/24/2013
Labeler - NDC National Distribution & Contracting, Inc. (009831413)
Establishment
NameAddressID/FEIOperations
Dukal088520668manufacture(43128-128)

 
NDC National Distribution & Contracting, Inc.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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