PRO ADVANTAGE INSTANT HAND SANITIZER- alcohol gel

Pro Advantage Instant Hand Sanitizer by

Drug Labeling and Warnings

Pro Advantage Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by NDC National Distribution & Contracting, Inc., Dukal. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

PRO ADVANTAGE INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43128-118
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	620 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
DMDM HYDANTOIN (UNII: BYR0546TOW)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43128-118-04	1 in 1 PACKAGE	03/08/2013
1		237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 43128-118-05	296 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/08/2013

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)

Establishment
Name	Address	ID/FEI	Business Operations
Dukal		088520668	manufacture(43128-118)