Medication Guide App

Clean Force Foam Hand Sanitizer

Dosage form: solution
Ingredients: BENZALKONIUM CHLORIDE 1mg in 1mL
Labeler: Ecolab Inc.
NDC Code: 47593-410

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 palmful
  • Spread to cover hands, rub in well
  • Air dry, do not rinse or towel dry

Other Information
  • READ SAFETY DATA SHEET (SDS) BEFORE USING THIS PRODUCT
  • 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, FDC red 40, FDC blue 1

Questions? call 1.866.444.7450

Principal Display Panel and Representative Label

MONOGRAM™  CLEAN FORCE®

CLEANING DISPOSABLES

FOAM HAND SANITIZER

648499

Hand Care

8000180

25 FL OZ (750 mL)

H16

Active Ingredient: Benzalkonium chloride 0.1%

CLEAN FORCE FOAM HAND SANITIZER 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-410
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:47593-410-41750 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/27/2003
Labeler - Ecolab Inc. (006154611)

Revised: 03/2015
 
Ecolab Inc.

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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