Megaplast Feet Wart Removal

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 Wart Removal
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 (until wart is removed) for up to 12 weeks.

Storage and handling

Store below 30ºC (66ºF)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 40%

OTC - PURPOSE SECTION

Wart Removal

WARNINGS SECTION

For External Use Only

OTC - DO NOT USE SECTION

Do not use

  • If you are diabetic
  • If you are pregnant
  • if you have poor blood circulation
  • for women who breastfeed
  • for children younger than 16 years old
  • on irritated skin or any area that is infected or reddened
  • Do not use on moles, birthmarks, warts with hair growing, or warts on the face or mucous membranes

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 (until wart is removed) for up to 12 weeks.

Use

INDICATIONS & USAGE SECTION

to facilitate wart removal.

Wart patches help the removal of common and plantar warts as they adapt perfectly to the affected area. The patches provide effective occlusion therapy, thus facilitating wart removal. Moreover, they help to reduce the risk of bacterial infections and the spread of warts to other people or areas.

Water resistant.

STORAGE AND HANDLING SECTION

Store below 30ºC (66ºF)

INACTIVE INGREDIENT SECTION

Lactic Acid, Acrylic Copolymer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71235-00171235-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
be6203aa-e881-d94f-e053-2a95a90a0d78477dd4f0-d697-5d3b-e054-00144ff8d46c2021-03-25WarningsExact identifier
spl set id: 477dd4f0-d697-5d3b-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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