ANTISEPTIC TOWELETTE- benzalkonium chloride liquid

ANTISEPTIC by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredients

Benzalkonium Chloride 0.133%

Purpose

First Aid Antiseptic

Keep out of reach of children.

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 without soap and water. Air dries in seconds.

WARNINGS:

For external use only. Do not use in or around the eyes.

Directions

Tear open packet, unfold and use as a washcloth.

Stop Use

if irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

Inactive Ingredients

Kathon CG, Water

Antiseptic Towelette Label WET NAP bulk product Label

MAX

PACKAGING

NDC: 59647-750-01

Antiseptic Towelette

Contains Benzalkoniun Chloride

For External use Only

1 Towelette

MAX PACKAGING

Attalla, AL

(256) 538-543www.maxpackaging.com

Made in USA

EXP: 03/2018

LOT MN06916 ABC

WET NAP

60,000

MAX

ANTISEPTIC

LOT #15048 MAX-BZK

INGREDIENTS AND APPEARANCE

ANTISEPTIC  TOWELETTE
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59647-750
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.1 mg  in 1.4 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: 59647-750-00	60000 in 1 CONTAINER	02/15/2016
1	NDC: 59647-750-01	1.4 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	part333A	02/15/2016

Labeler - Med-Nap LLC (079086400)

Registrant - Med-Nap LLC (079086400)

Establishment
Name	Address	ID/FEI	Business Operations
Med-Nap LLC		079086400	manufacture(59647-750)