Retail Foaming Alcohol Hand Sanitizer by Kay Chemical Company Drug Facts

Retail Foaming Alcohol Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

RETAIL FOAMING ALCOHOL HAND SANITIZER - alcohol solution 
Kay Chemical Company

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Drug Facts

Active ingredient

Ethyl alcohol, 62% w/w (equivalent to 70% v/v)

Purpose

Antiseptic handwash

Uses

• for hand washing 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.

Do not use

• in eyes
  

When using this product

• if in eyes, rinse promptly and throughly with water
• discontinue use if irritation and redness develop
  

Stop use and ask doctor if skin irritation and redness persists from 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
• spread to cover hands thoroughly, rub to dry
  

Other information

• for additional information, see Safety Data Sheet (SDS)
• for emergency medical information in USA, call (877) 231+-2615 or call collect - (952) 853-1713

Inactive ingredients  water (aqua), PEG-10 dimethicone, ethylhexylglycerin, farnesol, bisabolol, tert-butyl alcohol, denatonium benzoate

Questions? call 1-800-529-5458

Principal display panel and representative label

NDC: 63146-312-09   ECOLAB

RETAIL

Foaming Alcohol

Hand Sanitizer

KEEP OUT OF REACH OF CHILDREN

Net contents:

40.6 US fl oz (1200 mL)

Active ingredient:

Ethyl alcohol 62% w/w (equivalent to 70% v/v)

SDS-NC-872, SDS-WI-15014, SDS-NJ-20007

Distributed by

Kay Chemical Company

8300 Capital Drive - Greensboro NC 27409-9790 USA

Customer Service: (800) 529-5458

(c)2020 Kay Chemical Company

All rights reserved

Made in USA

RETAIL FOAMING ALCOHOL HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63146-312
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BIS-PEG-12 DIMETHICONE (500 MPA.S) (UNII: 2CNS542YRT)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
FARNESOL (UNII: EB41QIU6JL)
.ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63146-312-09	1200 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/02/2020	12/31/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/02/2020	12/31/2025

Labeler - Kay Chemical Company (003237021)

Revised: 12/2025

Document Id: 1db6f380-0a33-42e3-9e47-87602626c9a6

34390-5

Set id: 8e7ff0be-1bdc-4c06-8296-628727bd24d3

Version: 4

Effective Time: 20251231