North Safety First Aid Kit 35P10BBK

Drug Labeling and Warnings

Drug Details [pdf]

NORTH SAFETY FIRST AID KIT 35P10BBK- benzalkonium chloride, ethyl alcohol 
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 35P10BBK

BZK TOWELETTE

Active Ingredients

Benzalkonium Chloride, 0.133%

BZK TOWELETTE

Purpose

First Aid Antiseptic

BZK TOWELETTE

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

BZK TOWELETTE

BZK TOWELETTE

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

BZK TOWELETTE

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

BZK TOWELETTE

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

BZK TOWELETTE

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

BZK TOWELETTE

Inactive Ingredients Sodium Bicarbonate, Water

PAWS WIPE

Active ingredients

Ethyl Alcohol 66.5%

PAWS WIPE

Purpose

Antiseptic

PAWS WIPE

Uses

• for handwashing to decrease bacteria on skin when soap and water is not available

PAWS WIPE

Warnings

For external use only

Flammable: keep away from fire or flame

PAWS WIPE

Do not use in the eyes. If this happens, rinse thoroughly with water.

PAWS WIPE

Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours

PAWS WIPE

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

PAWS WIPE

Directions

• tear open packet, remove towelette
• wipe hand/wrist areas for 15 seconds and discard
• supervise children under 6 years of age

PAWS WIPE

Inactive ingredients aloe vera, fragrance, purified water, triethanolamine

BZK TOWELETTE

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

PAWS WIPE

Safetec
NDC: 61010-3111-1
p.a.w.s.
Antimicrobial Hand Wipe
Kills 99.99% of Germs!
Enriched with Aloe Vera
Fresh Scent
1 Premoistened Towelette For Professional Use
SAFETEC OF AMERICA, Inc.
Buffalo, NY 14215 800-456-7077 www.safetec.com

NORTH SAFETY FIRST AID KIT 35P10BBK 
benzalkonium chloride, ethyl alcohol kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0498-8036

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0498-8036-99	1 in 1 KIT; Type 0: Not a Combination Product	09/22/2008	09/24/2019

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1053 PACKET	2 L  in .0019
Part 2	1 POUCH	1 mL  in 1.4

Part 1 of 2

ANTIMICROBIAL 
alcohol liquid

Product Information
Item Code (Source)	NDC: 61010-3111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	665 mL  in 1 L

Inactive Ingredients
Ingredient Name	Strength
ALOE (UNII: V5VD430YW9)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61010-3111-1	0.0019 L 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	part333E	09/22/2008

Part 2 of 2

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	09/22/2008

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/22/2008	09/24/2019

Labeler - Honeywell Safety Products USA, Inc (079287321)

Establishment
Name	Address	ID/FEI	Business Operations
Honeywell Safety Products USA, Inc		079287321	pack(0498-8036)

Revised: 9/2019

Document Id: 9354fe57-38c6-2a7c-e053-2a95a90ab63c

34390-5

Set id: 5b5da3d4-8400-8632-e053-2a91aa0aa23f

Version: 2

Effective Time: 20190924