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 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

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 Foaming Hand Soap

Active Ingredient: Benzalkonium chloride 0.5%

Sysco® 4596843 6101146 ECOLAB®

750 mL (25.3 US FL OZ) 764502/5401/0918

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

Representative label

KEYSTONE
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-561
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
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 900000 MW) (UNII: B70CUU14M9)
WATER (UNII: 059QF0KO0R)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
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)
MYRISTAMINE OXIDE (UNII: J086PM3RRT)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
GLYCERYL CAPRYLOCAPRATE (UNII: U72Q2I8C85)
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:47593-561-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/21/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	12/21/2016

Labeler - Ecolab Inc. (006154611)

Drug Facts