McD Hand Sanitizer

Dosage form: solution
Ingredients: ETHANOL 60mL in 100mL
Labeler: Kay Chemical Company
NDC Code: 63146-302

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 (in each use)

Ethanol, 60% by volume

Purpose

Antiseptic handwash

Uses
  • Antibacterial hand sanitizer

Warnings
  • For external use only.
  • FLAMMABLE. Keep away from sparks and open flame.

Do not use
  • In eyes
  • On deep cuts or puncture wounds

When using this product
  • Discontinue use if irritation and redness develop

Stop use and ask a doctor if
  • Eye or skin irritation and redness persist 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 liberal amount into hand
  • Spread by rubbing hands together
  • Rub to dryness with attention to area around nails and between fingers

Other information
  • THIS PRODUCT IS NOT A SUBSTITUTE FOR HANDWASHING WITH SOAP AND WATER
  • For additional information, see Material Safety Data Sheet (MSDS)
  • For emergency medical information in the USA call 1.800.328.0026 or call collect 1.651.222.5352 (in the USA)

Inactive ingredients

water, isopropyl alcohol, acrylates/C10-C30 alkyl acrylate crosspolymer, triethanolamine, propylene glycol, myristyl alcohol

Questions?

Call 1-800-35-CLEAN (352-5326)

Principal Display Panel/Representative Label

McD

Hand Sanitizer

To obtain Spanish instructions, see outer carton.

Made in the U.S.A. for exclusive use by McDonald's Restaurants

McDonald's Corporation, Oak Brook, IL 60523, USA

(11872)

KAY CHEMICAL COMPANY

Greensboro, NC 27409-9790, USA

McDonald's, McD and the Golden Arches Logo are trademarks of McDonald's Corporation and affiliates.

27 OZ (800 mL)

MCD HAND SANITIZER 
ethanol, 60% by volume solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63146-302
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ETHANOL (ETHANOL) ETHANOL60 mL  in 100 mL
Packaging
#Item CodePackage Description
1NDC:63146-302-02800 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33305/26/2010
Labeler - Kay Chemical Company (003237021)

Revised: 05/2010
 
Kay Chemical Company

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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