MCD HAND SANITIZER- ethanol, 60% by volume solution 
Kay Chemical Company

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.

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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)

Representative label

MCD HAND SANITIZER 
ethanol, 60% by volume solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63146-302
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
MYRISTYL ALCOHOL (UNII: V42034O9PU)  
TROLAMINE (UNII: 9O3K93S3TK)  
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63146-302-02800 mL in 1 BAG; Type 0: Not a Combination Product05/26/201003/16/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/26/201003/16/2018
Labeler - Kay Chemical Company (003237021)

Revised: 4/2018
Document Id: 27ec0565-4abc-4971-9423-07a432e87533
Set id: d9cf19eb-9d2f-4cfc-b0f3-c643139be007
Version: 2
Effective Time: 20180425
 
Kay Chemical Company