CLEAN FORCE FOAM HAND SANITIZER- benzalkonium chloride solution

Clean Force Foam Hand Sanitizer by

Drug Labeling and Warnings

Clean Force Foam Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Ecolab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 INGREDIENT

Inactive ingredients water (aqua), isopropyl alcohol, propylene glycol, FDC red 40, FDC blue 1

QUESTIONS

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

INGREDIENTS AND APPEARANCE

CLEAN FORCE FOAM HAND SANITIZER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-410
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-410-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/27/2003

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/27/2003

Labeler - Ecolab Inc. (006154611)