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

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Use

for handwashing to decrease bacteria on the skin

Warnings

• For external use only; hands only

When using this product

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

Stop use and ask a doctor if

  • Irritation and redness develops
  • Condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

  • wet hands
  • apply palmful to hands
  • scrub throughly
  • rinse throughly

Inactive Ingredients

Water, Cocamidopropyl Betaine, Lauramine Oxide, PEG-150 distearate, Sodium Chloride, cetrimonium chloride, decyl glucoside, glycerin, freagrance, disteareth-75 IPDI, citric acid, tetrasodium EDTA, DMDM hydantoin, benzophenone-4, yellow 5, red 40, red 33

REF: P778108 NDC 43128-108-02

Made in the USA with US and foreign components for:

NDC, Inc., 407 New Sanford Road, La Vergne, TN 37086
www.ProAdvantagebyNDC.com


Product Labels

NDC 43128-108-02

PRO ADVANTAGE ANTIBACTERIAL 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43128-108
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43128-108-021 in 1 PACKAGE02/07/201902/07/2019
1237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2NDC:43128-108-03296 mL in 1 BOTTLE; Type 0: Not a Combination Product02/07/201902/07/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/07/201902/07/2019
Labeler - NDC National Distribution & Contracting, Inc. (009831413)
Establishment
NameAddressID/FEIBusiness Operations
Dukal088520668manufacture(43128-108)

Revised: 3/2023
 
NDC National Distribution & Contracting, Inc.