Alcohol Gel Hand Sanitizer by Kay Chemical Company Drug Facts

Alcohol Gel Hand Sanitizer by

Drug Labeling and Warnings

Alcohol Gel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Kay Chemical Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALCOHOL GEL HAND SANITIZER- alcohol solution 
Kay Chemical Company

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Drug Facts

Active ingredient

Ethyl Alcohol 60% v/v

Purpose

Antiseptic handwash

Uses

  • For handwashing to decrease bacteria on skin
  • recommended for repeated use

Warnings

  • For external use only
  • Flammable, keep away from fire or flame, heat, sparks and sources of static discharge.

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 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 thoroughly with product and allow to dry without wiping.
  • do not use if hands are visibly dirty or greasy; wash hands with soap and water instead.

Other information

  • For additional information, see Safety Data Sheet (SDS)
  • EMERGENCY HEALTH INFORMATION: 1 877 231 2615. If located outside the United States and Canada, call collect 952 853 1713 (number is in the US).

Inactive ingredients

​water (aqua), isopropyl alcohol, triethanolamine, acrylates/C10-30 alkyl acrylate crosspolymer, propylene glycol, myristyl alcohol

Questions? Call 1-800-529-5458

Principal display panel and representative label

ECOLAB

NDC: 63146-318-16

Alcohol Gel Hand Sanitizer

Active Ingredient: Ethyl Alcohol 60% v/v

1200 mL (40.6 US FL OZ)

1112849

Kay Chemical Company · 8300 Capital Drive

Greensboro, NC 27409-9790 USA

Customer Service: (800) 529-5458

©2024 Kay Chemical Company

All rights reserved

KUSA

782984/8000/0224

SDS-NC-872

representative label

ALCOHOL GEL HAND SANITIZER 
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 63146-318
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
TROLAMINE (UNII: 9O3K93S3TK)  
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
MYRISTYL ALCOHOL (UNII: V42034O9PU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 63146-318-161200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/14/202412/31/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)06/14/202412/31/2025
Labeler - Kay Chemical Company (003237021)

Revised: 12/2025
 

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