NORTHSIDE HOSPITAL HAND SANITIZING- benzalkonium chloride liquid

NORTHSIDE HOSPITAL by

Drug Labeling and Warnings

NORTHSIDE HOSPITAL 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

Use:

Antiseptic Cleansing of face, hands and body.

Caution: Keep out of reach of children.

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

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 appopriately after single use.

Inactive Ingredients:

Water, Methylchloroisothiazolinone, Methylisothiazolinone

NORTHSIDE HOSPITAL - Instant hand sanitizing wipes - product label

NH

NORTHSIDE HOSPITAL

Instant hands sanitizing wipes
Hand washing reduces Infections

Latex Free

1 Pouch

NDC# 59647-748-01

See box for full Drug Facts information

LOT: MN17817      EXP: 05/19

Made in the USA for: Food Service Resources
www.fsrfoodservice.com      1 REV 0

INGREDIENTS AND APPEARANCE

NORTHSIDE HOSPITAL  HAND SANITIZING
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59647-748
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59647-748-00	1000 in 1 CONTAINER	07/05/2017
1	NDC: 59647-748-01	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	part333A	07/05/2017

Labeler - Med-Nap LLC (079086400)

Registrant - Med-Nap LLC (079086400)

Establishment
Name	Address	ID/FEI	Business Operations
Med-Nap LLC		079086400	manufacture(59647-748)