4268 First Aid Kit by Honeywell Safety Products USA, Inc. 4268 FIRST AID KIT kit

4268 First Aid Kit by

Drug Labeling and Warnings

4268 First Aid Kit by is a Otc medication manufactured, distributed, or labeled by Honeywell Safety Products USA, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl alcohol 66.5%

Purpose

Antiseptic

Uses

for handwashing to decrease bacteria on skin whenever soap and water is not readily available

Warnings

For external use only

Flammable: keep away from fire or flame

Do not use

• in the eyes. If this happens, rinse thoroughly with water.

Stop use and ask a doctor if

• irritation or redness develop and persists for more than 72 hours

Keep out of reach of children

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

Directions

• wet hands and wrists thoroughly for 15 seconds and allow to air dry
• always reseal after use
• children under 6 years of age should be supervised when using this product

Inactive ingredients

aloe vera, fragrance, purified water, triethanolamine

Questions

1-800-430-5490

BZK Active ingredient

Benzalkonium chloride 0.13% w/v

BZK Purpose

First aid antiseptic

BZK Uses

Antiseptic cleansing of face, hands, and body without soap and water

BZK Warnings

For external use only

Do not use

• in the eyes or over large areas of the body
• on mucous membranes
• on irritated skin
• in case of deep puncture wounds, animal bites or serious burns, consult a doctor
• longer than 1 week unless directed by a doctor

Stop use and ask a doctor if

• if irritation, redness or other symptoms develop
• the condition persists or gets worse

Keep out of reach of children

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

BZK Directions

• tear open packet and use as a washcloth

BZK Other information

• store at room temperature 15 0 to 30 0 C (59 0 - 86 0 F)
• do not reuse towelette

BZK Inactive ingredient

water

BZK Questions

1-800-430-5490

4268 SF00000669 Kit Contents

3 PAWS PERS ANTIMICRO WIPE

LBL STOCK 6-3/8"X4"

LBL STOCK 3"x1-7/8"

1 BZK ANTISEPTIC WIPE, BULK

2 PR LRG NITRILE GLVES ZIP BAG

1 FACEMASK W/SHLD EAR LOOP

1 PICK-UP SCOOP W/SCRAPER

1 SOLIDIFIER BBP POUCH 2 OZ ID E

1 KIT, PP 10 UNIT FA

2 BAG BIOHAZARD 24 X 24 RED

2 TOWEL 3-FOLD WHITE

2 TWIST TIE

PAWS Principal Display Panel

BZK Principal Display Panel

4268 Kit Label SF00000669

INGREDIENTS AND APPEARANCE

4268 FIRST AID KIT 
4268 first aid kit kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0498-4268

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0498-4268-01	1 in 1 KIT	10/13/2018

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	3 PACKET	0.0057 L
Part 2	1 PACKET	1.4 mL

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)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1		10 in 1 BOX
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	12/21/2017

Part 2 of 2

ANTISEPTIC TOWELETTE 
benzalkonium chloride liquid

Product Information
Item Code (Source)	NDC: 0498-0501
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 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0498-0501-00	1.4 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	part333E	12/21/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/13/2018

Labeler - Honeywell Safety Products USA, Inc. (079287321)

Registrant - Honeywell Safety Products US, Inc. (079287321)

Establishment
Name	Address	ID/FEI	Business Operations
Honeywell Safety products USA, Inc.		079287321	pack(0498-4268)

Establishment
Name	Address	ID/FEI	Business Operations
Changzhou Maokang Medical		421317073	manufacture(0498-0501)

Establishment
Name	Address	ID/FEI	Business Operations
Safetec of America		874965262	manufacture(61010-3111)