Active Ingredient

Benzalkonium chloride 0.5%

Purpose

Antiseptic handwash

Uses

for handwashing to decrease bacteria on the skin

Warning

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 physician 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

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, 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 1-866-781-8787

Representative Label and Principal Display Panel

KEYSTONE SYSCO

ADVANCED ANTIBACTERIAL FOAM HAND SOAP

Active ingredient: Benzalkonium chloride 0.5%

Sysco 5284789 6101971 ECOLAB®

Net Contents

750 mL (25.3 US FL OZ) 6101971

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

For SDS information visit:

www.cleawnwithkeystone.com

Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA

Made in United States

www.ecolab.com · 773738/5401/1018

Representative label

KEYSTONE
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-595
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 PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
MYRISTIC DIISOPROPANOLAMIDE (UNII: 17DN142CTK)
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	Marketing End Date
Packaging
1	NDC:47593-595-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/20/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	09/20/2018

Labeler - Ecolab Inc. (006154611)

Drug Facts