ECOLAB ADVANCED HAND SANITIZER- alcohol solution

Ecolab Advanced Hand Sanitizer by

Drug Labeling and Warnings

Ecolab Advanced 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

Ethyl alcohol 70% v/v (equivalent to 62.5% w/w)

Purpose

Antiseptic handwash

Uses

• For handwashing 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 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

• wash hands to remove soil
• dispense palmful
• spread to cover hands, rub in well
• air dry, do not rinse or towel dry

Other information

• for additional information, see Safety Data Sheet (SDS)
• EMERGENCY HEALTH INFORMATION: 1 800 328 0026. If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US).

INACTIVE INGREDIENT

​Inactive ingredients​ water (aqua), glycerin, acrylates/C10-30 alkyl acrylate crosspolymer, t-butyl alcohol, aminomethyl propanol, denatonium benzoate

QUESTIONS

​Questions? ​call ​1-800-35-CLEAN (352-5326)

Representative label and principal display panel

ECOLAB

ADVANCED

HAND SANITIZER

Alcohol Antiseptic

70% Topical Solution

Active Ingredient: Ethyl alcohol 70% v/v (equivalent to 62.5% w/w)

6102237

Net Contents:  3.78 L (1 US GAL)

Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA ·

tel: 1 800 35 CLEAN (352 5326)

© 2020 Ecolab USA Inc. · All rights reserved

Made in USA

www.ecolab.com · 777232/5400/0720

SDS-CA-15195

INGREDIENTS AND APPEARANCE

ECOLAB ADVANCED HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-636
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)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-636-81	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/17/2020
2	NDC: 47593-636-11	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/17/2020

Labeler - Ecolab Inc. (006154611)