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 product
scrub hands and forearms
rinse thoroughly and dry

Other information

for additional information, see Safety Data Sheet (SDS)
for emergency medical information in USA and Canada, call 1 800 328 0026

Inactive ingredients water (aqua), cocamine oxide, hexylene glycol, PEG-180, glycerin, hydroxyethylcellulose, cocamidopropyl PG-dimonium chloride phosphate, phenoxyethanol, myristamide DIPA, myristamine oxide, methyl gluceth-20, glyceryl caprylate/caprate, alcohol, PEG-12 dimethicone, citric acid, polyquatemium-7, fragrance, potassium hydroxide, blue 1

Questions? call 1-866-781-8787

Principal display panel and representative label

KEYSTONE Sysco

ADVANCED ANTIBACTERIAL LIQUID HAND SOAP

Active Ingredient: 0.5% Benzalkonium Chloride

Net Contents

750 mL (25 US fl oz) 6000234

Sysco 5287436 6101969 ECOLAB®

This product may be patented: www.ecolab.com/patents

For SDS information visit: www.cleanwithkeystone.com

Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA · tel: 1 800 35 CLEAN (352 5326)

Made in U.S.A.

www.ecolab.com · 773734/5400/0818

representative label

KEYSTONE
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-594
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)
HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
MYRISTIC DIISOPROPANOLAMIDE (UNII: 17DN142CTK)
MYRISTAMINE OXIDE (UNII: J086PM3RRT)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
ALCOHOL (UNII: 3K9958V90M)
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47593-594-11	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/06/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	09/06/2018

Labeler - Ecolab Inc. (006154611)

Drug Facts