QUIK-CARE- 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 handwashing to decrease bacteria on the skin
• Recommended for repeated use

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

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 throughly and rub until dry

Other information

• for additional information, see Material Safety Data Sheet (MSDS)
• for emergency medical information in USA, call 1 800 328 0026

INACTIVE INGREDIENT

Inactive ingredients water (aqua), PEG-10 dimethicone, ethylhexylglycerin, glycerin, C12-C15 alkyl benzoate, niacinamide, glycine, bisabolol, tocopheryl acetate, propylheptyl caprylate, dicaprylyl caprylate, tert-butyl alcohol, gluconic acid, potassium hydroxide, denatonium benzoate

QUESTIONS

Questions? call 1 866 781 8787

Principal Display Panel and Representative Label

ECOLAB®

NDC: 47593-500-57

QUIK-CARE®

Nourishing Foam Hand Sanitizer

Dye and Fragrance Free

CHG Compatible

Active Ingredient: 62% Ethyl Alcohol

6000042

Net Contents: 535 mL (18.1 fl oz)

Ecolab 370 Wabasha Street N

St. Paul, MN 55102-1390 USA

© 2012 Ecolab USA Inc. All rights reserved

Made in United States

www.ecolab.com 754298/8500/1212

SDS-WI-15014

INGREDIENTS AND APPEARANCE

QUIK-CARE 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-500
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	539.4 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
NIACINAMIDE (UNII: 25X51I8RD4)
GLYCINE (UNII: TE7660XO1C)
.ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
GLUCONIC ACID (UNII: R4R8J0Q44B)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-500-55	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2013
2	NDC: 47593-500-57	535 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2013
3	NDC: 47593-500-38	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2013
4	NDC: 47593-500-85	45 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2013
5	NDC: 47593-500-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2013
6	NDC: 47593-500-59	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2013	05/03/2018
7	NDC: 47593-500-56	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/01/2013

Labeler - Ecolab Inc. (006154611)