Megaplast - Feet Corn Protective Plasters

Manufacturer
EUROSIREL SPA
Effective date
2020-01-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:42:27

Label at a glance#

ProductMegaplast - Feet Corn Protective Plasters
Active ingredientSALICYLIC ACID
Label structure11 sections

Dosage and administration

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)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 40%

INACTIVE INGREDIENT SECTION

Lactic Acid, Chlorophyll, Acrylic copolymer

Use

INDICATIONS & USAGE SECTION

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 SECTION

For External Use Only.

OTC - DO NOT USE SECTION

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

DOSAGE & ADMINISTRATION SECTION

  • 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)

OTC - ASK DOCTOR SECTION

If discomfort persists, see your doctor or podiatrist.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

STORAGE AND HANDLING SECTION

Store below 30ºC (66ºF)

OTC - PURPOSE SECTION

Corn Removal.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71235-00371235-003-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
be62077d-9b17-4cc5-e053-2995a90a7fca477e0732-6842-6617-e054-00144ff8d46c2021-03-25WarningsExact identifier
spl set id: 477e0732-6842-6617-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.