Active Ingredient

Benzalkonium chloride 0.5%

Purpose

Antiseptic handwash

Uses

for handwashing to decrease bacteria on the skin

Warnings

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

READ SAFETY DATA SHEET (SDS) BEFORE USING THIS PRODUCT
EMERGENCY HEALTH INFORMATIN: 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), cocamine oxide, hexylene glycol, PEG-180, glycerin, cocamidopropyl , PG-dimonium chloride phosphate, phenoxyethanol, polyquaternium-7, myristamide DIPA, myristamine oxide, citric acid, methyl gluceth-20, glyceryl caprylate/caprate, alcohol, PEG-12 dimethicone, potassium citrate, fragrance, blue 1

Questions? call 1.866.444.7450

Principal display panel and representative label

MONOGRAM CLEANING DISPOSABLES

CLEAN FORCE

ADVANCED ANTIBACTERIAL 768067

FOAM HAND SOAP

HAND CARE

8000460

42.3 US FL OZ (1250 mL) H26

Active Ingredient:

Benzalkonium chloride 0.5%

771096/5402/0521

For questions or comments,

call 1-866-444-7450

Manufactured by

Ecolab - 1 Eclab Place

St. Paul MN 55102 USA

Made in U.S.A.

Distributed by

US Foods Inc.

Rosemont, IL 60018 USA

representative label

CLEAN FORCE
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-584
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	5 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
GLYCERIN (UNII: PDC6A3C0OX)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
MYRISTIC DIISOPROPANOLAMIDE (UNII: 17DN142CTK)
MYRISTAMINE OXIDE (UNII: J086PM3RRT)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
ALCOHOL (UNII: 3K9958V90M)
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)
POTASSIUM CITRATE (UNII: EE90ONI6FF)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47593-584-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/30/2017
2	NDC:47593-584-59	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/30/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	06/30/2017

Labeler - Ecolab Inc. (006154611)

Drug Facts