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QSR Hand Sanitizer

Medically reviewed by Drugs.com. Last updated on May 22, 2020.

Dosage form: solution
Ingredients: ALCOHOL 534mg in 1mL
Labeler: Kay Chemical Company
NDC Code: 63146-112

Drug Facts

Active ingredient

Ethanol 60% by volume

Purpose

Antiseptic handwash

Uses
  • For handwashing to decrease bacteria on 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
  • on deep cuts or puncture wounds

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
  • Eye or 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
  • Apply a 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 Safety Data Sheet (SDS)
  • For emergency medical information in USA, call (877) 231-2615 or call collect 0 (952) 853-1713

Inactive ingredients

​water (aqua), isopropyl alcohol, triethanolamine, acrylates/C10-30 alkyl acrylate crosspolymer, propylene glycol, myristyl alcohol

Questions? Call 1-800-529-5458

Principal Display Panel/Representative Label

NDC 63146-112-09

KAY

QSR Hand Sanitizer

Keep out of reach of children • For institutional use only

Ethanol 60% by volume

Net contents: 40.6 US fl oz (1200 ml)

Meets the requirements for Hand Antiseptics as specified in section 2-301.16 of the 2009 Model Food Code.

​Distributed by:

KAY CHEMICAL COMPANY • 8300 Capital Drive

Greensboro, NC 27409-9790 USA

Customer Service: (800) 529-5458

©2016 Kay Chemical Company

All Rights Reserved

756614-01 • KUSA 756614/8001/0916

SDS-WI-15014

QSR HAND SANITIZER 
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63146-112
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL534 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ISOPROPYL ALCOHOL 
TROLAMINE 
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) 
PROPYLENE GLYCOL 
MYRISTYL ALCOHOL 
Packaging
#Item CodePackage Description
1NDC:63146-112-02800 mL in 1 BAG
2NDC:63146-112-0737 mL in 1 BOTTLE, PLASTIC
3NDC:63146-112-08750 mL in 1 BOTTLE
4NDC:63146-112-091200 mL in 1 BOTTLE
5NDC:63146-112-141000 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/23/2010
Labeler - Kay Chemical Company (003237021)

Document Id: cfa25bb7-558f-40db-972b-59fbe0136793
Set id: 4921e19c-08af-42cb-8df4-d6933e4598b2
Version: 7
Effective Time: 20200522
 
Kay Chemical Company

Further information

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

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