MED NAP - benzalkonium chloride liquid 
Med-Nap LLC

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.

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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

MedNap BZK1

MedNap BZK2

MED NAP  
benzalkonium chloride liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:59647-245
Route of Administration TOPICAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1.7 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
MAGNESIUM CHLORIDE ANHYDROUS (UNII: 59XN63C8VM)  
MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:59647-245-01 100 in 1 BOX 09/09/2013
1 NDC:59647-245-00 1.7 mL in 1 PACKET; Type 0: Not a Combination Product
2 NDC:59647-245-02 1000 in 1 BOX 09/09/2013
2 NDC:59647-245-00 1.7 mL in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 09/09/2013
Labeler - Med-Nap LLC (079086400)
Registrant - Med-Nap LLC (079086400)
Establishment
Name Address ID/FEI Business Operations
Med-Nap LLC 079086400 manufacture(59647-245)

Revised: 11/2016
Document Id: faba983e-59aa-48ea-94ac-d7f06cb34789
Set id: a304b40f-4886-4fee-bd4d-fe33c7bf2c0b
Version: 4
Effective Time: 20161110
 
Med-Nap LLC