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Kay Foaming Hand Sanitizer

Dosage form: solution
Ingredients: BENZALKONIUM CHLORIDE 0.1mL in 100mL
Labeler: Kay Chemical Company
NDC Code: 63146-109

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

Benzalkonium chloride 0.1%

Purpose

Antiseptic handwash

Uses
  • For handwashing to decrease bacteria on the skin

Warnings

For external use only

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 and 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
  • wash hands to remove soil
  • dispense palmful
  • spread to cover hands, rub in well
  • air dry, do not rinse or towel dry

Other Information
  • for additional information, see Material Safety Data Sheet (MSDS)
  • Medical emergency:  (877) 231-2615 or call collect 0 (952) 853-1713.

Inactive ingredients  water (aqua), isopropyl alcohol, propylene glycol, FDC Red 40, FDC Blue 1

Questions?  Call 1-800-529-5458

Principal Display Panel and representative label

NDC NO: 63146-109-06

KAY

Foaming Hand Sanitizer

See inside the back label for complete drug facts panel

Benzalkonium chloride 0.1%

40.6 US fl oz (1200 ml)

752776-00 KUSA 752776/8000/0611   copyright 2011 Kay Chemical Company   All rights reserved.




KAY FOAMING HAND SANITIZER 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63146-109
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.1 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ISOPROPYL ALCOHOL 
PROPYLENE GLYCOL 
FD&C RED NO. 40 
FD&C BLUE NO. 1 
Packaging
#Item CodePackage Description
1NDC:63146-109-03750 mL in 1 BOTTLE, PLASTIC
2NDC:63146-109-061200 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/22/2008
Labeler - Kay Chemical Company (003237021)

Revised: 09/2011
Document Id: fe16dfd7-5d42-44c9-9314-157c82672e3f
Set id: 43df5310-0302-4e6c-8e48-a35ae2d4c690
Version: 4
Effective Time: 20110914
 
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 drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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