Active Ingredient

Ethyl alcohol 54.7 w/w (equivalent to 62.5% 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.
Contents under pressure. Do not store at temperatures above 120°F (48°C), puncture or incinerate
Operate only with spout pointing down

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 develop 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

Apply product onto hands, spread thoroughly and rub until dry

Other Information

for additional information, see Safety Data Sheet (SDS)
for emergency medical informatnio in the USA, call 1-800-328-0026

Inactive Ingredients water (aqua), isobutane, glycerin, hydrofluorocarbon 152A, cetearyl alcohol, polysorbate-60, propane, sodium lauroyl lactylate, steareth-20, sodium benzoate, tert-butyl alcohol, denatonium benzoate

Questions? Call 1-866-781-8787

Representative Label and Principal Display Panel

ECOLAB®

47593-490-82

QUIK-CARE Aerosol Foam Hand Sanitizer

Clinically proven to promote skin health

Active Ingredient: 57.4% w/w (equivalent to 62.5% v/v)

6032713

Net Contents: 198 g (7 oz)

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

Made in United States

www.ecolab.com · 714083/8503/1022

SDA-MA-1396, SDS-IN-1561

DOT 2Q M5655

Representative Label

QUIK-CARE
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-490
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	54.7 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
Water (UNII: 059QF0KO0R)
isobutane (UNII: BXR49TP611)
GLYCERIN (UNII: PDC6A3C0OX)
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYSORBATE 60 (UNII: CAL22UVI4M)
PROPANE (UNII: T75W9911L6)
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
STEARETH-20 (UNII: L0Q8IK9E08)
SODIUM BENZOATE (UNII: OJ245FE5EU)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47593-490-82	198 g in 1 CAN; Type 0: Not a Combination Product	10/10/2012
2	NDC:47593-490-87	425 g in 1 CAN; Type 0: Not a Combination Product	10/10/2012

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	10/10/2012

Labeler - Ecolab Inc. (006154611)

Drug Facts