KAY ACTIGEL HAND SANITIZER- ethanol solution

Kay Actigel Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Ethanol 60% by volume

Purpose

Antiseptic handwash

Uses

• For handwashing to decrease bacteria on the skin

Warnings

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

Do not use

• In eyes
• On deep cuts or puncture wounds
  

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

• Eye or skin irritation and redness persist 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

• Apply liberal amount into hand
• Spread by rubbing hands together
• Rub to dryness with attention to area around nails and between fingers
  

Other information

• THIS PRODUCT IS NOT A SUBSTITUTE FOR HANDWASHING WITH SOAP AND WATER
• For additional information, see Material Safety Data Sheet (MSDS)
• For emergency medical information in the USA call 1 (877) 231-2615 or call collect 0 (952)853-1713

Inactive ingredients

water (aqua), isopropyl alcohol, triethanolamine, acrylates/C10-C30 alkyl acrylate crosspolymer, propylene glycol, myristyl alcohol

QUESTIONS

​Questions? call 1-800-529-5458

Principal Display Panel/Representative Label

Kay

Actigel

Hand Sanitizer

To obtain instruction in Spanish, see outer carton.

ECOLAB

KAY CHEMICAL COMPANY

8300 Capital Drive

Greensboro, NC 27409-9790, USA

Customer Service: (800) 529-5458

SDS-NC-872

27 US fl oz (800 ml)

722473-03

FRSUSA 722473/8003/0910

©2010 Kay Chemical Company

All Rights Reserved

INGREDIENTS AND APPEARANCE

KAY ACTIGEL HAND SANITIZER 
ethanol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-679
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: 47593-679-25	800 mL in 1 BAG; Type 0: Not a Combination Product	12/31/2025
2	NDC: 47593-679-21	208000 mL in 1 DRUM; Type 0: Not a Combination Product	12/31/2025

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

Labeler - Ecolab Inc. (006154611)