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PureForce by Ecolab Inc.

Medically reviewed on July 26, 2018

Dosage form: solution
Ingredients: BENZALKONIUM CHLORIDE 5mg in 1mL
Labeler: Ecolab Inc.
NDC Code: 47593-568

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 0.5%

Purpose

Antiseptic handwash

Uses
  • for handwashing to decrease bacteria on the skin

Warning ´╗┐For external use only

Do not use
  • in eyes

When using the 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
  • wet hands and apply foam
  • scrub hands and forearms
  • rinse thoroughly and dry

Other information
  • for additional information, see Safety Data Sheet (SDS)
  • for emergency medical information in USA and Canada, call 1 800 328 0026

Inactive ingredients water (aqua), cocamine oxide, hexylene glycol, PEG-180, glycerin, cocamidopropyl PG-dimonium chloride phosphate, myristamine oxide, phenoxyethanol, polyquaternium 7, citric acid, myristamide DIPA, methyl gluceth-20, caprylic/capric glycerides, PEG-12 dimethicone, potassium hydroxide, fragrance, FD&C blue 1

Questions? call 1-866-444-7450

Representative Label and Principal Display Panel

Advanced Antibacterial

Foaming Hand Soap

Hand Care

Cuidado de las manos

Active ingredient Benzalkonium chloride 0.5%

Ingrediente activo: Cloruro de benzalkonium 0.5%

766424/7100/0616

Product No.

8000329

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:47593-568
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
FD&C BLUE NO. 1 
POTASSIUM HYDROXIDE 
PEG-12 DIMETHICONE (300 CST) 
MEDIUM-CHAIN TRIGLYCERIDES 
METHYL GLUCETH-20 
MYRISTIC DIISOPROPANOLAMIDE 
CITRIC ACID MONOHYDRATE 
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 900000 MW) 
PHENOXYETHANOL 
MYRISTAMINE OXIDE 
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE 
GLYCERIN 
POLYETHYLENE GLYCOL 8000 
HEXYLENE GLYCOL 
WATER 
COCAMINE OXIDE 
Packaging
#Item CodePackage Description
1NDC:47593-568-591250 mL in 1 BOTTLE, PLASTIC
2NDC:47593-568-41750 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/26/2016
Labeler - Ecolab Inc. (006154611)

 
Ecolab Inc.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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