AMERICAN RED CROSS FIRST AID KIT- alcohol, benzalkonium chloride, bacitracin zinc, neomycin sulfate, polymyxin b sulfate, alcohol kit

American Red Cross First Aid Kit by

Drug Labeling and Warnings

American Red Cross First Aid Kit by is a Otc medication manufactured, distributed, or labeled by Tomy International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl Alcohol, 70% v/v...............        Purpose: Antiseptic

Use

    For preparation of skin before injection.

Warnings

For external use only.

STORAGE AND HANDLING

Flammable - keep away from fire or flame

Store at room temperature 15-30 degree Celsius (59-86 degree Fahrenheit)

Do not use:

with electrocautery, in the eyes.

STOP USE

Stop use if irritation and redness develop. If condition persists for more than 72 hours, consult your doctor.

Keep out of reach of children

If swallowed,

get medical help or contact a Poison Control

Center right away.

WHEN USING

Wipe Injection site vigorously and discard.

Inactive Ingredient

Purified water.

DESCRIPTION

LOT/EXP:                Made in CHINA

20140301

PRINCIPAL DISPLAY PANEL

Alcohol Cleansing  Pad
Genuine First Aid LLC, Clearwater FL 33755

www.GenuineFirstAid.com

1/pouch

GENUINE FIRST AID

Active Ingredient

Bacitracin Zinc 400 units

Neomycin Sulfate 5mg ( equivalent to 3.5 mg Neomycin base)

Polymyxin B Sulfate 5000 units

Uses:

To help prevent infection in:
minor cuts;  scrapes;  burns

Warnings>

For external use only.

Do not use

in eyes;  over large areas of the body;

If allergic to any of the ingredients;  for more than one week unless directed by a physician.

Stop use and consult a doctor

if the condition persists or gets worse;  a rash or other allergic reaction develops

Keep out of reach of children

If ingested, contact a Poison

Control Center right away.

Directions

Cclean affected area;  apply small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily; may be covered with a sterile bandage

Other Information

Store at room temperature.

PRINCIPAL DISPLAY PANEL

Genuine Triple Antibiotic

First Aid Ointment

To Help Prevent Infection

Each Gram Contains:

Bacitracin Zinc 400 units

Neomycin Sulfate 5 mg

(equivalent to 3.5 mg

Neomycin base)

 Polymyxin B Sulfate 5000 units

Net Wt. 0.5g ; (1/64 oz)

Manufactured in CHINA for

GENUINE FIRST AID.

Active Ingredint

Benzalkonium Chloride 0.40%..........   Purpose: First Aid Antiseptic

Use

For Professional and Hospital use.  Helps prevent infection.  Antiseptic cleansing of face, hands and body without soap and water.

Warning

For external use only.

Keep out of reach of children

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

STOP USE

Stop use if unusual redness, swelling or other symptoms occur. Consult a physician immediately.

DO NOT USE

Do not use in the eyes or over large areas of the body.

WHEN USING

Directions: Tear open packet, unfold towelette and use to cleanse desired skin area.  Discard towelette appropriately after single use.

Inactive Ingredient

Purified water

DESCRIPTION

LOT/EXP:                           Made in CHINA

20130301

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antimicrobial

Uses

For handwashing to decrease bacteria on the skin.

Warnings

For external use only.

Flammable

Do not use

in the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and consult a doctor

if irritation and redness develop and persist for more than 72 hours

Directions

Empty contents into palm. Rub hands until gel dissipates. Recommended for repeated use.

Inactive Ingredients

Propylene glycol, carbomer, titanium dioxide, purified water

Keep out of reach of children

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

PRINCIPAL DISPLAY PANEL

Genuine Hand Sanitizer

Instant Gel

Antiseptic Handwash with Vitamin E and Aloe

Kills 99.9% of germs without water

Active Ingredient:

Ethyl alcohol 62%

Net Wt 0.9g (1/32oz)

PRINCIPAL DISPLAY PANEL

Antiseptic Towelette

Genuine First Aid LLC, Clearwater FL 33755

www.GenuineFirstAid.com

1/pouch

GENUINE FIRST AID

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AMERICAN RED CROSS FIRST AID KIT 
alcohol, benzalkonium chloride, bacitracin zinc, neomycin sulfate, polymyxin b sulfate, alcohol kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42354-7482

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42354-7482-4	1 in 1 KIT

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	2 TUBE	1.0 g
Part 2	2 PACKAGE	1.6 mL
Part 3	4 PACKAGE	2.0 mL
Part 4	2 PACKET	1.8 g

Part 1 of 4

GENUINE TRIPLE ANTIBIOTIC 
bacitracin zinc,neomycin sulfate,polymyxin b sulfate ointment

Product Information
Item Code (Source)	NDC: 52124-0003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN ZINC	400 [iU]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN SULFATE	5 mg  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B SULFATE	5000 [iU]  in 1 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52124-0003-1	.5 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333B	01/11/2011

Part 2 of 4

ANTISEPTIC TOWELETTE 
benzalkonium chloride swab

Product Information
Item Code (Source)	NDC: 52124-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.40 mL  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52124-0001-1	0.8 mL in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333E	01/11/2011

Part 3 of 4

ALCOHOL CLEANSING PAD 
isopropyl alcohol liquid

Product Information
Item Code (Source)	NDC: 52124-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52124-0002-1	0.5 mL in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/11/2011

Part 4 of 4

GENUINE HAND SANITIZER 
alcohol gel

Product Information
Item Code (Source)	NDC: 52124-2906
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52124-2906-1	0.9 g in 1 PACKET

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/28/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/17/2012

Labeler - Tomy International (065183758)