PRO ADVANTAGE INSTANT HAND SANITIZER- alcohol liquid

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]

Drug Facts

ACTIVE INGREDIENT:

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: P779114 NDC:

43128-114-03

Made in China
www.ProAdvantagebyNDC.com

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

PRINCIPAL DISPLAY PANEL

Pro Advantage by NDC Instant
Hand Sanitizer
4 FL. OZ.
( 118 mL )
Kills Germs With 62% Alcohol
*+M220P77911480*

Product Labels

INGREDIENTS AND APPEARANCE

PRO ADVANTAGE INSTANT HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43128-114
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: 43128-114-03	1 in 1 PACKAGE	03/08/2013
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product

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(43128-114)