QUIK-CARE- ethyl alcohol solution

Quik-Care by

Drug Labeling and Warnings

Quik-Care 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 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 INGREDIENT

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

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

© 2019 Ecolab USA Inc · All rights reserved

Made in United States

www.ecolab.com · 714083/8501/1019

SDA-MA-1396

DOT 2Q M5655

INGREDIENTS AND APPEARANCE

QUIK-CARE 
ethyl alcohol solution

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

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

Inactive Ingredients
Ingredient Name	Strength
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
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 Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/10/2012

Labeler - Ecolab Inc. (006154611)