PRO ADVANTAGE ANTIBACTERIAL - triclosan liquid 
NDC National Distribution & Contracting, Inc.

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.

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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 Blue #1

REF: P778108 NDC 43128-108-02

Made in China
www.ProAdvantagebyNDC.com

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

Product Labels

Liquid Soap Label

PRO ADVANTAGE ANTIBACTERIAL 
triclosan liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:43128-108
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 3 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
COCAMINE OXIDE (UNII: QWA2IZI6FI)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43128-108-02 1 in 1 PACKAGE
1 237 mL in 1 BOTTLE, PUMP
2 NDC:43128-108-03 296 mL in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 03/08/2013
Labeler - NDC National Distribution & Contracting, Inc. (009831413)

Revised: 4/2013
Document Id: c669a212-3efd-424e-8538-8106b613ae25
Set id: 9f53b063-4e55-4be6-a8f4-b8c9d2341eba
Version: 3
Effective Time: 20130424
 
NDC National Distribution & Contracting, Inc.