KEYSTONE- benzalkonium chloride solution

Keystone by

Drug Labeling and Warnings

Keystone 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 0.5%

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 INGREDIENT

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

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

© 2018 Ecolab USA Inc. · All rights reserved

Made in United States

www.ecolab.com · 773738/5401/1018

INGREDIENTS AND APPEARANCE

KEYSTONE 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-595
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-595-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/20/2018

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

Labeler - Ecolab Inc. (006154611)