PRO ADVANTAGE INSTANT HAND SANITIZER  - alcohol 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.

----------

Pro Advantage Instant Hand Sanitizer

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

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

Product Labels

Hand Sanitizer Label

PRO ADVANTAGE INSTANT HAND SANITIZER  
alcohol liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:43128-114
Route of Administration TOPICAL DEA Schedule     
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)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43128-114-03 1 in 1 PACKAGE
1 118 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: 3/2013
Document Id: d9a4bd1d-cf81-45f2-9161-4aae74dbd9b7
Set id: a430c9f9-5510-4f75-8ddf-9c625f139e52
Version: 2
Effective Time: 20130327
 
NDC National Distribution & Contracting, Inc.