North Safety First Aid Kit 019740-0027L / Z019740-0027L

Drug Labeling and Warnings

Drug Details [pdf]

NORTH SAFETY FIRST AID KIT 019740-0027L/Z019740-0027L- benzalkonium chloride 
Honeywell Safety Products LLC

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 019740-0027L / Z019740-0027L

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

NORTH SAFETY FIRST AID KIT 019740-0027L/Z019740-0027L 
benzalkonium chloride kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0498-8043

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0498-8043-99	1 in 1 KIT; Type 0: Not a Combination Product	04/01/2004	09/24/2019
2	NDC: 0498-8043-98	1 in 1 KIT; Type 0: Not a Combination Product	04/01/2004	09/24/2019

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 POUCH	1 mL  in 1.4

Part 1 of 1

BZK TOWELETTE 
benzalkonium chloride swab

Product Information
Item Code (Source)	NDC: 65517-0004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.33 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65517-0004-1	1.4 mL in 1 POUCH; 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	04/01/2004

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/01/2004	09/24/2019

Labeler - Honeywell Safety Products LLC (079287321)

Establishment
Name	Address	ID/FEI	Business Operations
Honeywell Safety Products USA, Inc		079287321	pack(0498-8043)

Revised: 9/2019

Document Id: 9354fe57-38a2-2a7c-e053-2a95a90ab63c

34390-5

Set id: 5b3518c6-f388-4814-e053-2991aa0a2bfb

Version: 2

Effective Time: 20190924