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PureForce by Ecolab Inc.

Medically reviewed on January 6, 2017

Dosage form: solution
Ingredients: BENZALKONIUM CHLORIDE 1mg in 1mL
Labeler: Ecolab Inc.
NDC Code: 47593-567

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

Warnings
  • For external use only

Do not use
  • In eyes

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
  • skin irritation or redness occurs 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
  • Wash hands to remove soil
  • Dispense 20 mL into hand (palmful)
  • Spread to cover hands, rub in well for at least 30 seconds
  • Air dry, do not rinse or towel dry

Other Information
  • For additional information, see Safety Data Sheet (SDS)
  • EMERGENCY HEALTH INFORMATION: 1 800 328 0026. If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US).

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

Foodservice Foaming

Hand Sanitizer

Hand Care

Cuidado de las manos

Active ingredient: Benzalkonium Chloride 0.1%

766499/7100/0616

Product No.

8000340

42.3 US FL OZ (1250 mL)

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

Distributed by
PureForce
370 Wabasha Street N
St Paul MN 55102-1390 USA
© 2016 Ecolab USA Inc
All rights reserved
Made in U.S.A.

PUREFORCE 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-567
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:47593-567-41750 mL in 1 BOTTLE, PLASTIC
2NDC:47593-567-591250 mL in 1 BOTTLE, PLASTIC
3NDC:47593-567-30207 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/14/2016
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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