KAY FOAMING HAND SANITIZER- benzalkonium chloride solution

Kay Foaming Hand Sanitizer by

Drug Labeling and Warnings

Kay Foaming Hand Sanitizer 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 0.1%

Purpose

Antiseptic handwash

Uses

• For handwashing to decrease bacteria on the skin
  

Warnings

For external use only

Do not use

• In eyes
  

When using this 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 and 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

• wash hands to remove soil
• dispense palmful
• spread to cover hands, rub in well
• air dry, do not rinse or towel dry
  

Other Information

• for additional information, see Safety Data Sheet (SDS)
• Medical emergency:  (877) 231-2615 or call collect 0 (952) 853-1713

INACTIVE INGREDIENT

Inactive ingredients  water (aqua), isopropyl alcohol, propylene glycol, CI 16035 (FD&C Red 40), CI 42090 (FD&C Blue 1)

QUESTIONS

Questions?  Call 1-800-529-5458

Principal Display panel and representative label

KAY

Foaming Hand Sanitizer

KEEP OUT OF REACH OF CHILDREN - FOR INSTITUTIONAL USE ONLY

Benzalkonium chloride 0.1%

Net contents: 42 US fl oz (1250 ml)

Distributed by:

Kay Chemical Company  8300 Capital Drive

Greensboro, NC 27409-9790  USA

Customer Service: (800) 529-5458

©2018 Kay Chemical Company

All rights reserved

757547-02 KUSA 757547/8002/0618

INGREDIENTS AND APPEARANCE

KAY FOAMING HAND SANITIZER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-670
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-670-59	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/17/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/17/2025

Labeler - Ecolab Inc. (006154611)