MEGAPLAST - FEET CORN PROTECTIVE PLASTERS- salicylic acid plaster

Megaplast - Feet Corn Protective Plasters by

Drug Labeling and Warnings

Megaplast - Feet Corn Protective Plasters 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%

INACTIVE INGREDIENT

Lactic Acid, Chlorophyll, Acrylic copolymer

Use

For the removal of hard corns. Before applying, carefully clean and dry the area to be protected to ensure perfect adhesion and effectiveness. Remove corn plaster from paper and position it centrally over the area to be protected. Apply a new corn plaster daily.

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 breastfeed
• 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.

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)

ASK DOCTOR

If discomfort persists, see your doctor or podiatrist.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

STORAGE AND HANDLING

Store below 30ºC (66ºF)

PURPOSE

Corn Removal.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MEGAPLAST - FEET CORN PROTECTIVE PLASTERS 
salicylic acid plaster

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71235-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2.068 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: 71235-003-01	17 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(71235-003)