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Quik-Care by Ecolab Inc.

Medically reviewed on May 3, 2018

Dosage form: solution
Ingredients: Alcohol 539.71mg in 1mL
Labeler: Ecolab Inc.
NDC Code: 47593-491

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

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

Principal display panel and representative label

ECOLAB®

QUIK-CARE®

Foam Hand Sanitizer

NDC 47593-491-41

Dye and Fragrance Free

CHG Compatible

Active Ingredient: 62% Ethyl Alcohol

Net Contents: 750mL (25 fl oz)

6000073

US Patent Numbers: 8,383,686,B2; 8,058,315 and 7,842,725

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

© 2013 Ecolab USA Inc · All rights reserved

Made in United States

755128/8500/0413

SDS-WI-15014

QUIK-CARE 
ethyl alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-491
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (ALCOHOL) Alcohol539.71 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
PEG-10 DIMETHICONE (600 CST) 
ETHYLHEXYLGLYCERIN 
FARNESOL 
.ALPHA.-BISABOLOL, (+/-)- 
TERT-BUTYL ALCOHOL 
DENATONIUM BENZOATE 
Packaging
#Item CodePackage Description
1NDC:47593-491-551000 mL in 1 BOTTLE, PLASTIC
2NDC:47593-491-41750 mL in 1 BOTTLE, PLASTIC
3NDC:47593-491-38500 mL in 1 BOTTLE, PLASTIC
4NDC:47593-491-8545 mL in 1 BOTTLE, PLASTIC
5NDC:47593-491-561200 mL in 1 BOTTLE, PLASTIC
6NDC:47593-491-57535 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/19/2013
Labeler - Ecolab Inc. (006154611)

 
Ecolab Inc.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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