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MED NAP

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1.3mg in 1.7mL
Labeler: Med-Nap LLC
NDC Code: 59647-245

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.

Benzalkonium Chloride Towelette - 245

Drug Facts
Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

First Aid Antiseptic

Caution:

Keep out of reach of children.

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

Use:

Antiseptic Cleansing of face, hands and body.

Warnings


For External Use Only.

Do not use in or around the eyes.

Do not apply over large area of the body.

Stop use

if irritation, redness or other symptoms  develop.

Consult a doctor if the condition persists or gets worse.

Directions

Tear open packet, unfold towelette and use to cleanse desired skin area. Discard towelette appropriately after a single use.

Inactive Ingredients

Water, Kathon CG

MED NAP BENZALKONIUM CHLORIDE TOWELETTE

MED NAP

Record No. 3303

NDC # 59647-245-01

BZK
ANTISEPTIC
TOWELETTE

LatexFree

1 Pouch

Made by:
MED-NAP LLC,
Brooksville, FL 34601

www.mednap.us

Recorder No. 3303

Made in the USA

* See box for full Drug Facts information

Lot: 16325 E F G    EXP: 10/2018

Made In USA  1 REV 3

MED NAP  
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59647-245
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.3 mg  in 1.7 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
MAGNESIUM CHLORIDE ANHYDROUS 
MAGNESIUM NITRATE 
Packaging
#Item CodePackage Description
1NDC:59647-245-01100 PACKET in 1 BOX
1NDC:59647-245-001.7 mL in 1 PACKET
2NDC:59647-245-021000 PACKET in 1 BOX
2NDC:59647-245-001.7 mL in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E09/09/2013
Labeler - Med-Nap LLC (079086400)
Registrant - Med-Nap LLC (079086400)
Establishment
NameAddressID/FEIOperations
Med-Nap LLC079086400manufacture(59647-245)

Revised: 11/2016
 
Med-Nap 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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