PUREFORCE- alcohol solution

Pureforce by

Drug Labeling and Warnings

Pureforce by is a Otc medication manufactured, distributed, or labeled by Ecolab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

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 sparks and open flame.
  

Do not use

• in eyes
• on deep cuts or puncture wounds
  

When using this product

• if in eyes, promptly and throughly 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
  

INACTIVE INGREDIENT

Inactive ingredients  water, isopropyl alcohol, triethanolamine, acrylates/C10-30 alkyl acrylate crosspolymer, propylene glycol, myristyl alcohol

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 USA and Canada, call 1.800.328.0026
• For emergency medical information worldwide, call 1.651.222.5352 (in USA)

QUESTIONS

Questions? call 1.866.444.7450

Principal display panel and representative label

PureForce

Hand Sanitizer

Hand Care

G

Use  Pureforce Hand Sanitizer to sanitize hands

between handwashings.

Product No.

8000055

Net Contents: 27 fl oz/800 mL

For questions or comments,

call 1-866-444-7450

www.pureforcesvc.com

Distribute by:

PureForce

370 Wabasha Street North

St. Paul, MN 55102

copyright 2010 PureForce

All Rights Reserved

Made in U.S.A.

749946/7100/0610

INGREDIENTS AND APPEARANCE

PUREFORCE 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-473
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: 47593-473-25	800 mL in 1 POUCH; Type 0: Not a Combination Product	04/27/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/27/2011

Labeler - Ecolab Inc. (006154611)