MEGAPLAST - FEET CORN REMOVAL PLASTER- salicylic acid plaster

Megaplast - Feet Corn Removal Plaster by

Drug Labeling and Warnings

Megaplast - Feet Corn Removal Plaster by is a Otc medication manufactured, distributed, or labeled by EUROSIREL SPA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 40%

Use

• For removal of hard corns. These corn plasters with a central disc in polyethylene foam perform a smoothing and protective action, softening the skin and facilitating its mechanical removal, thus ensuring fast and pain-free corn removal. Moreover, their thickness protects the affected area against rubbing and pressure.

WARNINGS

For External Use Only.

DO NOT USE

Do not use

• if you are diabetic
• if you have poor blood circulation
• if you are pregnant
• for women who breast feed
• for children younger than 16 years old
• on irritated skin or on any area that is infected or reddened

Do not use for more than two weeks.

ASK DOCTOR

If discomfort persists, see your doctor or podiatrist.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Directions

• Wash affected area and dry thoroughly
• Apply medicated plaster. After 48 hours remove the medicated plaster. Repeat this procedure every 48 hours as needed for up to 14 days (until corn is removed).

STORAGE AND HANDLING

• Store below 30ºC (66ºF)

INACTIVE INGREDIENT

Lactic Acid, Chlorophyll, Acrylic copolymer

PURPOSE

Corn Removal.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MEGAPLAST - FEET CORN REMOVAL PLASTER 
salicylic acid plaster

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71235-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	3.175 mg

Inactive Ingredients
Ingredient Name	Strength
LACTIC ACID (UNII: 33X04XA5AT)
CHLOROPHYLL (UNII: 00WNZ48OR9)
ACRYLIC ACID/ISOPHORONE DIISOCYANATE/PEG-27 COPOLYMER (UNII: R0R8I3X29J)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71235-002-01	6 in 1 BOX; Type 0: Not a Combination Product	07/14/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358F	07/14/2017

Labeler - EUROSIREL SPA (655512069)

Registrant - EUROSIREL SPA (655512069)

Establishment
Name	Address	ID/FEI	Business Operations
EUROSIREL SPA		655512069	manufacture(71235-002)