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Quik-Care by Ecolab Inc.

Dosage form: solution
Ingredients: ALCOHOL 620mg in 1mL
Labeler: Ecolab Inc.
NDC Code: 47593-457

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%

Purpose

Antiseptic handwash

Healthcare personnel handwash

Uses
  • For hand washing to decrease bacteria on the skin

Warnings
  • For external use only
  • FLAMMABLE. Keep away from fire, heat, sparks, and sources of discharge.

Do not use
  • in eyes

When using this product
  • avoid contact with eyes and mucous membranes
  • if in eyes, rinse promptly and thoroughly with water

Stop use and ask a doctor if skin iirritation or redness occurs and persists for more than 72 hours.

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center immediately.

Directions
  • Apply 1-2 pumps of product to hands
  • Spread thoroughly and rub until dry

Other Information
  • Keep away from fire or flame
  • Do not store above 120oF (50oC)
  • For emergency medical information in USA/Canada, call 1.800.328.0026 or worldwide, call 1.651.222.5352 (in USA)

Inactive ingredients water (aqua), glycerin, tetrahydroxypropyl ethylenediamine, ethylhexylglycerin, isopropyl palmitate, acrylates/C10-30 alkyl acrylate crosspolymer, C12-15 alkyl benzoate, panthenol, dimethicone, tocopheryl acetate, aloe barbadensis leaf juice.

Questions?  Call 1.866.781.8787

Principal Display Panel/Representative Label

ECOLAB®

Quik-Care Moisturizing Gel Waterless Antimicrobial Hand Sanitizer

Enriched with More Moisturizers for Improved Skin Health

62% Ethyl Alcohol

One-Step procedure, no rinse required

Net Contents:  18 U.S. fl oz/540 mL

Ecolab Inc.

370 Wabasha Street N.

St. Paul, MN 55102

Made in U.S.A.

SDA-WI-2509

© 2008 Ecolab Inc.

All Rights Reserved

716285/8500/1107

Reorder #61073540

QUIK-CARE  
ethyl alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-457
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL620 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER  
GLYCERIN 
EDETOL 
ETHYLHEXYLGLYCERIN 
ISOPROPYL PALMITATE 
CARBOMER COPOLYMER TYPE A 
C12-20 ALKYL BENZOATE 
PANTHENOL 
DIMETHICONE 
.ALPHA.-TOCOPHEROL ACETATE, D- 
ALOE VERA LEAF 
Packaging
#Item CodePackage Description
1NDC:47593-457-321000 mL in 1 BOTTLE, PLASTIC
2NDC:47593-457-261000 mL in 1 BAG
3NDC:47593-457-33118 mL in 1 BOTTLE, PLASTIC
4NDC:47593-457-31540 mL in 1 BOTTLE, PLASTIC
5NDC:47593-457-551000 mL in 1 BOTTLE, PLASTIC
6NDC:47593-457-4937 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/29/2008
Labeler - Ecolab Inc. (006154611)

Revised: 03/2016
 
Ecolab Inc.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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