Megaplast - Feet Corn Removal Plaster

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 Removal Plaster
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%

Use

INDICATIONS & USAGE SECTION

  • 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 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 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.

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.

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).

STORAGE AND HANDLING SECTION

  • Store below 30ºC (66ºF)

INACTIVE INGREDIENT SECTION

Lactic Acid, Chlorophyll, Acrylic copolymer

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
71235-00271235-002-01

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
be620621-4ab2-dd64-e053-2a95a90a536c477e0732-683f-6617-e054-00144ff8d46c2021-03-25WarningsExact identifier
spl set id: 477e0732-683f-6617-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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