ESC PROTECTING FOAM HAND SANITIZER- alcohol solution

ESC Protecting Foam Hand Sanitizer by

Drug Labeling and Warnings

ESC Protecting Foam 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% w/w (equivalent to 76.9% v/v)

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 eye or 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: 1 800 328 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), isopropyl alcohol, PEG-10 dimethicone, glycerin, ethylhexylglycerin, myristyl alcohol, niacinamide, tocopheryl acetate

Questions?

call 1-800-35-CLEAN (352-5326)

Representative label and principal display panel

ECOLAB SCIENTIFIC CLEAN

PROTECTING FOAM

HAND SANITIZER

1200 mL

(40.6 US FL OZ) 6102899

Active ingredient: Ethyl alcohol 70% w/w (equivalent to 76.9% v/v)

Ecolab Inc · 1 Ecolab Place · St. Paul MN 55102 USA · tel: 1 800 35 CLEAN (352 5326)

© 2025 Ecolab USA Inc. · All rights reserved

Made in U.S.A.

www.ecolab.com · 785031/5400/0825

SDS-NJ-20007, SDA-MN-914, SDS-WI-20072

INGREDIENTS AND APPEARANCE

ESC PROTECTING FOAM HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-667
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	76.9 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
BIS-PEG-12 DIMETHICONE (500 MPA.S) (UNII: 2CNS542YRT)
GLYCERIN (UNII: PDC6A3C0OX)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
MYRISTYL ALCOHOL (UNII: V42034O9PU)
NIACINAMIDE (UNII: 25X51I8RD4)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-667-56	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/29/2025
2	NDC: 47593-667-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/29/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/29/2025

Labeler - Ecolab Inc. (006154611)