KNOCKOUT HAND SANITIZER

Dosage form: solution
Ingredients: Alcohol 42mg in 25mL
Labeler: Midway Advanced Products, LLC
NDC Code: 52490-200

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.

KNOCKOUT™
HAND SANITIZER

Drug Facts

Active ingredient

Ethyl Alcohol 62% w/w

Purpose

Antimicrobial

Uses

To sanitize hands without water. Kills 99% of most common bacteria.

Warnings

Flammable.

For external use only.

Keep away from fire or flame.

Do not use in the eyes.

Discontinue use if irritation or redness develop.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Tear open packet and apply entire amount of gel to unsoiled hands. Rub in thoroughly until hands are dry. Do not wipe or use water rinse.

Other information

Store at room temperature.

Inactive ingredients

Water, Carbomer, Diisopropylamine, Polysorbate 80, Cetyl Acetate, Acetylated lanolin Alcohol, Propylene Glycol, Diazolidinyl Urea, Methylparaben, Propylparaben.

Distributed by
Midway Advanced Products, LLC
1-713-722-5460

PRINCIPAL DISPLAY PANEL - 1.2 ml Packet

TEAR HERE

KNOCKOUT™

HAND SANITIZER

KILLS GERMS | ANTIBACTERIAL

Benefiting Service Members

B4products.com
1.2 ml net contents

KNOCKOUT  HAND SANITIZER
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52490-200
Route of AdministrationPERCUTANEOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (Alcohol) Alcohol42 mg  in 25 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Diisopropylamine 
Polysorbate 80 
Propylene Glycol 
Diazolidinyl Urea 
Methylparaben 
Propylparaben 
Packaging
#Item CodePackage Description
1NDC:52490-200-1625 PACKET (PACKET) in 1 CASE
11.2 mL in 1 PACKET
2NDC:52490-200-1750 PACKET (PACKET) in 1 CASE
21.2 mL in 1 PACKET
3NDC:52490-200-18100 PACKET (PACKET) in 1 CASE
31.2 mL in 1 PACKET
4NDC:52490-200-19200 PACKET (PACKET) in 1 CASE
41.2 mL in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E08/01/2011
Labeler - Midway Advanced Products, LLC (962765009)

Revised: 08/2011
 
Midway Advanced Products, LLC

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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