MED NAP- benzalkonium chloride liquid

MED NAP by

Drug Labeling and Warnings

MED NAP by is a Otc medication manufactured, distributed, or labeled by Med-Nap LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug FactsActive 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

INGREDIENTS AND APPEARANCE

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)