ALCOHOL GEL HAND SANITIZER- alcohol solution

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]

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

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

INGREDIENTS AND APPEARANCE

ALCOHOL GEL HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63146-318
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63146-318-16	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/14/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/14/2024

Labeler - Kay Chemical Company (003237021)