KAY HAND SANITIZER FOAM- ethyl alcohol solution

Kay Hand Sanitizer Foam by

Drug Labeling and Warnings

Kay Hand Sanitizer Foam by is a Otc medication manufactured, distributed, or labeled by Ecolab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl alcohol 54.7 w/w (equivalent to 62.5% v/v)

Purpose

Antiseptic Handwash

Uses

• For handwashing to decrease bacteria on the skin

Warnings

• For external use only
• Flammable, keep away from fire or flame, heat, sparks and sources of static discharge.
• Contents under pressure. Do not store at temperatures above 120°F (48°C), puncture or incinerate
• Operate only with spout pointing down

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 or redness develop 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

• Spread thoroughly onto hands and rub until 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), isobutane, glycerin, cetearyl alcohol, hydrofluorocarbon 152A, propane, polysorbate-60, sodium lauroyl lactylate, steareth-20, sodium benzoate, tert-butyl alcohol, denatonium benzoate

QUESTIONS

Questions? Call 1-800-529-5458

Representative Label and Principal Display Panel

KAY®

Hand Sanitizer Foam

Net Contents: 425 g (15 oz)

Active Ingredient: 54.7% w/w (equivalent to 62.5% v/v)

1110978

ECOLAB

This product may be patented | Este producto

puede ser patentado: www.ecolab.com/patents

Distributed by | Distribuido por:

Kay Chemical Company · 8300 Capital Drive

Greensboro, NC 27409-9790 USA

Customer Service: (800) 529-5458

©2022 Kay Chemical Company

All rights reserved | Todas los derechos reservados

Made in USA | Hecho en Estados Unidos

822113 KUSA 775938/8001/1122

INGREDIENTS AND APPEARANCE

KAY HAND SANITIZER FOAM 
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-683
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	54.7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
isobutane (UNII: BXR49TP611)
GLYCERIN (UNII: PDC6A3C0OX)
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYSORBATE 60 (UNII: CAL22UVI4M)
PROPANE (UNII: T75W9911L6)
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
STEARETH-20 (UNII: L0Q8IK9E08)
SODIUM BENZOATE (UNII: OJ245FE5EU)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-683-96	425 g in 1 CAN; 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)