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Pro Advantage Instant Hand Sanitizer

Medically reviewed on Jan 11, 2018

Dosage form: gel
Ingredients: ALCOHOL 620mg in 1mL
Labeler: NDC National Distribution & Contracting, Inc.
NDC Code: 43128-118

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 Instant Hand Sanitizer Gel

Pro Advantage Instant Hand Sanitizer Gel


Active Ingredients:

Alcohol 62%

Purpose

Antiseptic

Use

To help reduce bacteria on the hands that can potentially cause disease.

Warning:

• For External Use Only
• Flammable, keep away from fire or flame.

When using this product

• Avoid contact with eyes, if this occurs rinse thoroughly with water and contact a physician.

Ask a doctor before use if you have

• Deep wounds, animals bites or serious burns.

Stop use and ask a doctor if

• Condition persists.

Keep out of reach of children.

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

Directions:

Apply a liberal amount to hands and rub hands thoroughly until dry. Do not rinse or wipe off gel.

Inactive Ingredients:

Water, Glycerin, Fragrance, Carbomer, Triethanolamine, DMDM Hydantoin

REF: P779118 NDC 43128-118-04

Made in China
www.ProAdvantagebyNDC.com

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

Product Labels

PRO ADVANTAGE INSTANT HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43128-118
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL620 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERIN 
TROLAMINE 
DMDM HYDANTOIN 
Packaging
#Item CodePackage Description
1NDC:43128-118-041 BOTTLE, PUMP in 1 PACKAGE
1237 mL in 1 BOTTLE, PUMP
2NDC:43128-118-05296 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/08/2013
Labeler - NDC National Distribution & Contracting, Inc. (009831413)
Establishment
NameAddressID/FEIOperations
Dukal088520668manufacture(43128-118)

 
NDC National Distribution & Contracting, Inc.

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Further information

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

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