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Ecolab Inc. by Ecolab Inc.

Dosage form: solution
Ingredients: BENZALKONIUM CHLORIDE 8.9mg in 1mL
Labeler: Ecolab Inc.
NDC Code: 47593-514

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 0.89%


Antispetic handwash

  • For handwashing to decrease bacteria on the skin

  • 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 Posoin Control Center right away.

Directions: Concentrated Solution
  • do not mix with anything except for potable water
  • use only provided bottles for dilution and dispensing of ready-to-use product
  • remove cap, open dispenser door, place bottle into position, and close dispenser door
  • fill hand sanitizer bottle with solution from dispenser
  • place bottle into a Nexa dispenser for use

Directions: Ready-To-Use Solution
  • wash hands to remove soil
  • apply sanitizer to hands
  • spread to cover hands thoroughly, rub to 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), propylene glycol, ethanol, sodium benzoate, FD&C yellow 5, FD&C red 40

Questions? call1-800-35-CLEAN (352-5326)

Principal Display Panel and Representative Label

ECOLAB®     6100874


Concentrated Foam Hand Sanitizer

1.3 L (44 US FL OZ)

Active ingredient: Benzalkonium chloride, 0.89%

benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-514
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 
#Item CodePackage Description
1NDC:47593-514-621300 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/02/2015
Labeler - Ecolab Inc. (006154611)

Revised: 03/2015
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.