ALLSEASON ANTIBACTERIAL BANDAGE- benzalkonium chloride dressing

AllSeason Antibacterial Bandage by

Drug Labeling and Warnings

AllSeason Antibacterial Bandage by is a Otc medication manufactured, distributed, or labeled by Excellence Medical Supplies Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Benzalkonium Chloride 0.9g /m2

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses

For use in minor cuts, scrapes and burns.Proper care is important to avoid infections or future complications.

DOSAGE & ADMINISTRATION

Directions:

For optimal results, apply bandage to clean, dry skin. Change the dressing daily, when wet, ot more often if needed.

WARNINGS

Warning:

For external use only. In case of deep cut, puncture wounds, animal bites, or serious burns,consult a doctor if the condition persists or gets worse.

Keep this and all drugs out of reach of children

Do not Use:

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

Do not use longer than one week unless directed by a doctor

Stop Use:

If adhere to the skin, and if individual person has an allergy with it, stop use it.

ASK DOCTOR

Consult a doctor if the condition persists or gets worse.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center immediately.

SPL UNCLASSIFIED SECTION

Other Information

Store at room temperature

Avoid excessive heat (above 40C)

Protect from freezing

Latex free

INACTIVE INGREDIENT

Inactive Ingredient:

HDPE, Cellulose

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALLSEASON ANTIBACTERIAL BANDAGE 
benzalkonium chloride dressing

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72306-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.28 mg  in 3.125 cm2

Inactive Ingredients
Ingredient Name	Strength
ALPHA CELLULOSE (UNII: I355QGZ19A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72306-001-01	30 in 1 PACKAGE	06/05/2018
1		3.125 cm2 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	part333E	06/05/2018

Labeler - Excellence Medical Supplies Co., Ltd. (527730762)

Registrant - Excellence Medical Supplies Co., Ltd. (527730762)

Establishment
Name	Address	ID/FEI	Business Operations
Excellence Medical Supplies Co., Ltd.		527730762	manufacture(72306-001)