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Kool and Kleen Antiseptic Towelette

Dosage form: cloth
Ingredients: Benzalkonium Chloride 0.13mg in 100mL
Labeler: Medline Industries, Inc.
NDC Code: 53329-930

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

Purpose

First Aid Antiseptic

Use

As a First Aid Antiseptic to help prevent infection in minor cuts, scrapes and burns

Warnings

For external use only

Do not use
  • in the eyes or apply over large areas of the body
  • longer than 1 week unless directed by a doctor

Stop use and ask a doctor if
  • condition persists or gets worse
  • you have deep or puncture wounds, animal bites or serious burns

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions
  • Clean the affected area
  • Apply a small amount of this product on the area 1 to 3 times daily
  • May be covered with a sterile bandage
  • If bandaged, let dry first

Storage

Store at room temperature: 20 to 25 degrees C (68 to 77 degrees F)

Inactive ingredients

Isopropyl Alcohol, Fragrance, Propylene Glycol, Sodium Bicarbonate, Water

Questions

1-800-MEDLINE

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Benzalkonium Chloride Antiseptic Towelette

KOOL AND KLEEN ANTISEPTIC  TOWELETTE
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-930
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (Benzalkonium) Benzalkonium Chloride0.13 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Isopropyl Alcohol 
Propylene Glycol 
Sodium Bicarbonate 
Water 
Packaging
#Item CodePackage Description
1NDC:53329-930-992000 PACKET in 1 CASE
11 APPLICATOR in 1 PACKET
15 mL in 1 APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/200708/31/2017
Labeler - Medline Industries, Inc. (025460908)

Revised: 08/2012
 
Medline Industries, Inc.

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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