CLEAN FORCE FOAM HAND SANITIZER - benzalkonium chloride solution 
Ecolab Inc.

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%

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

Distributed by:                           © 2015 Ecolab USA Inc

PureForce                                  All Rights Reserved

370 Wabasha Street North          Made in U.S.A

St. Paul, MN 55102                    755506/7100/0115

image description

CLEAN FORCE FOAM HAND SANITIZER 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-410
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47593-410-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/27/2003
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/27/200305/31/2023
Labeler - Ecolab Inc. (006154611)

Revised: 5/2023
Document Id: d283cb9a-4040-45a2-94c2-499a4f6b5eee
Set id: 29bc0ea4-5fb1-4903-8ad9-4bd091da6b9e
Version: 5
Effective Time: 20230531
 
Ecolab Inc.