Medication Guide App

Quik-Care Waterless Antimicrobial Foaming Hand Rub

Dosage form: solution
Ingredients: Ethanol 54.7g in 100g
Labeler: Ecolab Inc.
NDC Code: 47593-280

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, 62.5% v/v

Purpose

Antiseptic handwash

Uses
  • Antiseptic foam hand rinse

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 120oF (48oC), 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 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
  • Spread thoroughly onto hands 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
  • For emergency medical information worldwide, call 1.651.222.5352 (in the USA)

Inactive ingredients

water (aqua), isobutane, glycerin, cetearyl alcohol, hydrofluorocarbon 152A, propane, polysorbate-60, sodium lauryl lactylate, steareth-20, sodium benzoate

Questions? Call 1.866.781.8787

Principal Display Panel/Representative Label

ECOLAB

Quik-Care

Waterless Antimicrobial Foaming Hand Rub

SDA-MA-1396

DIN 02241735

Net Contents:  7 0z (198 g)

Active Ingredient:  62.5% Ethyl Alcohol

  • Kills germs fast
  • One-step procedure, no rinse required
QUIK-CARE  WATERLESS ANTIMICROBIAL FOAMING HAND RUB
antiseptic handwash solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-280
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Ethanol (Ethanol) Ethanol54.7 g  in 100 g
Packaging
#Item CodePackage Description
1NDC:47593-280-82198 g in 1 CAN
2NDC:47593-280-87425 g in 1 CAN
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33305/06/1999
Labeler - Ecolab Inc. (006154611)

Revised: 11/2009
 
Ecolab Inc.

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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