NORTHSIDE HOSPITAL HAND SANITIZING- 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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Northside Hospital (hand san wipe) - 748

Drug Facts
Active 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

Med-Nap NH handsan

NORTHSIDE HOSPITAL  HAND SANITIZING
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59647-748
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1.7 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59647-748-001000 in 1 CONTAINER07/05/2017
1NDC:59647-748-011.7 mL in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/05/2017
Labeler - Med-Nap LLC (079086400)
Registrant - Med-Nap LLC (079086400)
Establishment
NameAddressID/FEIBusiness Operations
Med-Nap LLC079086400manufacture(59647-748)

Revised: 7/2017
Document Id: 58e348f8-29fb-45d4-8a90-dd3cc329e04b
Set id: 8a103698-bbf1-4512-a635-e3709180026b
Version: 1
Effective Time: 20170707
 
Med-Nap LLC