MOSCO

Manufacturer
Medtech Products Inc.
Effective date
2017-12-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:06:34

Label at a glance#

ProductMOSCO
Active ingredientSALICYLIC ACID
Label structure10 sections

Dosage and administration

wash affected area may soak corn in warm water for 5 minutes dry thoroughly remove medicated pad from backing paper by pulling from center of pad apply repeat procedure every 48 hours as needed for up to 14 days (until corn is removed)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 40%

Purpose

OTC - PURPOSE SECTION

Corn remover

Use

INDICATIONS & USAGE SECTION

For the removal of corns

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • on irritated skin
  • on any area that is infected or reddened
  • if you have diabetes or poor blood circulation
OTC - STOP USE SECTION
Stop use and ask a doctor

OTC - ASK DOCTOR SECTION

if discomfort persists

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wash affected area
  • may soak corn in warm water for 5 minutes
  • dry thoroughly
  • remove medicated pad from backing paper by pulling from center of pad
  • apply
  • repeat procedure every 48 hours as needed for up to 14 days (until corn is removed)

Other information

SPL UNCLASSIFIED SECTION

  • store at room temperature
  • avoid excessive heat

Inactive ingredients

INACTIVE INGREDIENT SECTION

lanolin, polybutene, rosin ester, rubber

Questions?

OTC - QUESTIONS SECTION

1-800-443-4908

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MOSCO Maximum Strength One Step Corn Remover Pads

Salicylic Acid 40%

8 Pads

MOSCO One Step Corn Remover Pads CartonMOSCO One Step Corn Remover Pads Carton

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63029-31063029-310-08

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
4219432d-7e4f-45a5-8c3c-11d11fff182a54a93082-0980-4431-ba65-3e048bfb6aa82024-12-11WarningsExact identifier
spl set id: 54a93082-0980-4431-ba65-3e048bfb6aa8

Reported adverse events (FAERS/openFDA)#

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