North Safety First Aid Kit Z130023L

Drug Labeling and Warnings

Drug Details [pdf]

NORTH SAFETY FIRST AID KIT Z130023L- benzalkonium chloride 
Honeywell Safety Products USA, Inc

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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North Safety First Aid Kit Z130023L

Active Ingredients

Benzalkonium Chloride, 0.133%

Purpose

First Aid Antiseptic

Use Antiseptic Cleansing of face, hands and body without soap and water. Air dries in seconds.

Do Not Use in the eyes or apply over large areas of the body.

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

Caution Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions Tear open packet, unfold and use as a washcloth.

Inactive Ingredients Sodium Bicarbonate, Water

DUKAL CORPORATION

BZK TOWELETTE

Contains Benzalkonium Chloride

For External Use Only

1/Pouch

DUKAL CORPORATION (631) 656-3800

Ronkonkoma, NY www.dukal.com

Made in China

Dukal BZK TWLT Front

Dukal BZK TWLT Back

NORTH SAFETY FIRST AID KIT Z130023L 
benzalkonium chloride kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 0498-8051
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 0498-8051-991 in 1 KIT; Type 0: Not a Combination Product06/19/200609/24/2019
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 17 POUCH 10 mL  in 1.4 
Part 1 of 1
BZK TOWELETTE 
benzalkonium chloride swab
Product Information
Item Code (Source)NDC: 65517-0004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.33 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 65517-0004-11.4 mL in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/19/2006
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/19/200609/24/2019
Labeler - Honeywell Safety Products USA, Inc (079287321)
Establishment
NameAddressID/FEIBusiness Operations
Honeywell Safety Products USA, Inc079287321pack(0498-8051)

Revised: 9/2019
Document Id: 9356388f-0ba9-7a55-e053-2995a90a9fce
Set id: 5b46a32d-f06b-5d78-e053-2991aa0a7c84
Version: 2
Effective Time: 20190924