KEYSTONE LIQUID HAND SANITIZER- alcohol solution

Keystone Liquid Hand Sanitizer by

Drug Labeling and Warnings

Keystone Liquid Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Ecolab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each use)

Ethanol, 60% by volume

Purpose

Antiseptic handwash

Uses

• for handwashing to decrease bacteria on the skin
  

Warnings

• For external use only
• FLAMMABLE. Keep away from fire or flame, heat, sparks and sources of static discharge.

Do not use

• in eyes
• on deep cuts or puncture wounds

When using this product

• If in eyes, rinse promptly and thoroughly with water
• Discontinue use if irritation and redness develop

Stop use and ask a doctor if

• eye or skin irritation and redness persist 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

• apply liberal amount into hand
• spread by rubbing hands together
• rub to dryness with attention to area around nails and between fingers
  

Other information

• THIS PRODUCT IS NOT A SUBSTITUTE FOR HANDWASHING WITH SOAP AND WATER
• For additional information, see Material Safety Data Sheet (MSDS)
• For emergency medical information in the USA call 1.800.328.0026 or call collect 1.651.222.5352 (in the USA)
  

INACTIVE INGREDIENT

Inactive ingredients water, isopropyl alcohol, triethanolamine, acrylates/C10-C30 alkyl acrylate crosspolymer, propylene glycol, myristyl alcohol

QUESTIONS

Questions? call 1-800-35-CLEAN (352-5326)

Principal Display Panel and Representative Label

Keystone

Liquid Hand Sanitizer

Sysco 8509558             6100220 ECOLAB

Net Contents: 800 mL   748589/5401/0912

Distributed by Sysco Corporation

Ecolab - 370 Wabasha Street N - St. Paul, MN 55102-1390 USA - tel. 1 800 352 5326

©2012 Ecolab USA Inc. - All rights reserved

Made in United States   SDS-NC-872

INGREDIENTS AND APPEARANCE

KEYSTONE LIQUID HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-466
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
MYRISTYL ALCOHOL (UNII: V42034O9PU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-466-25	800 mL in 1 BAG; Type 0: Not a Combination Product	05/26/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/26/2010

Labeler - Ecolab Inc. (006154611)