KAY CHEMICAL HAND SANITIZER FOAM- ethyl alcohol solution 
Kay Chemical

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active Ingredient

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

Purpose

Antiseptic Handwash

Uses

Warnings

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

Other Information

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? 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

Representative Label

KAY CHEMICAL HAND SANITIZER FOAM 
ethyl alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63146-309
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL54.7 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63146-309-13425 g in 1 CAN; Type 0: Not a Combination Product04/23/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/23/2020
Labeler - Kay Chemical (003237021)

Revised: 11/2022
Document Id: 725a8b11-6046-4fd5-88b6-731a2599734a
Set id: 981405a0-ba34-4aa0-b0a8-d74cd2427dd1
Version: 3
Effective Time: 20221128
 
Kay Chemical