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, 62% w/w

Purpose

Antiseptic handwash

Uses

• for hand washing 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

• irritation and 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

• Apply product onto hands, spread thoroughly and rub until dry

Other Information

• for additional information, see Material Safety Data Sheet (MSDS)
• for emergency medical information in USA and Canada, call 1.800.328.0026

Inactive Ingredients

water (aqua), PEG-10 dimethicone, ethylhexylglycerin, farnesol, bisabolol, tert-butyl alcohol, denatonium benzoate

QUESTIONS

Questions? call 1.866.781.8787 24 hours a day, 7 days a week

Principal display panel and representative label

NDC: 47593-491-41

ECOLAB®

QUIK-CARE

Foam Hand Sanitizer

Dye and Fragrance Free

CHG Compatible

Active Ingredient: 62% Ethyl Alcohol

Net Contents: 750mL (25 fl oz)

6000073

This product may be patented: www.ecolab.com/patents

Ecolab · 370 Wabasha Street N · St Paul MN 55102-1390 USA

© 2020 Ecolab USA Inc · All rights reserved

Made in United States - 755128/8502/0320

SDS-WI-15014, SDS-NJ-20007, SDA-MA-1396

INGREDIENTS AND APPEARANCE

QUIK-CARE 
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-491
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	Alcohol	539.71 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
FARNESOL (UNII: EB41QIU6JL)
.ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-491-55	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/19/2013
2	NDC: 47593-491-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/19/2013
3	NDC: 47593-491-38	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/19/2013
4	NDC: 47593-491-85	45 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/29/2014
5	NDC: 47593-491-56	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/19/2013
6	NDC: 47593-491-57	535 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/09/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/19/2013

Labeler - Ecolab Inc. (006154611)