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PureForce by Ecolab Inc.

Medically reviewed on August 24, 2017

Dosage form: solution
Ingredients: BENZALKONIUM CHLORIDE 1mg in 1mL
Labeler: Ecolab Inc.
NDC Code: 47593-496

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.

Drug Facts

Active ingredient

Benzalkonium chloride 0.1%

Purpose

Antiseptic handwash

Uses
  • for handwashing to decrease bacteria on the skin
  • recommended for repeated use

Warnings

​For external use only

Do not use
  • in eyes

When using this product
  • if in eyes, rinse promptly and throughly with water
  • discontiue use if irritation and redness develop

Sto use and ask a doctor if
  • skin iritation or redness occurs for more than 72 hours

​Keep out of reach of children.​ If swallowed, get meidcal help or contact a Poison Control Center right away.

Directions
  • wash hands to remove soil
  • dispense palmful
  • spread to cover hands, rub in well
  • air dry, do not rinse or towel dry

Other information
  • for additional infromation, see Material Safety Data Sheet (MSDS)
  • for emergency medical information in USA and Canada, call 1.800.328.0026

​Inactive ingredients​ water (aqua), isopropyl alcohol, propylene glycol, FD&C red 40, FD&C blue 1

​Questions?​ call​ 1.866.444.7450

Principal display panel and representative label

Economy

Foam Hand Sanitizer

8000149

Net Contents:

750 ml (25 US fl oz)

For questions or comments, call 1-866-444-7450

Distributed by:

PureForce

370 Wabasha Street North

St. Paul, MN 55102

© 2012 Ecolab USA Inc.

All Rights Reserved

Made in U.S.A.

718767/7100/0612

PUREFORCE 
benzalkonium solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-496
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ISOPROPYL ALCOHOL 
PROPYLENE GLYCOL 
FD&C RED NO. 40 
FD&C BLUE NO. 1 
Packaging
#Item CodePackage Description
1NDC:47593-496-41750 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/23/2012
Labeler - Ecolab Inc. (006154611)

 
Ecolab Inc.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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