FDA.reportPublic FDA data

Compound W Complete Coverage Callus Remover

Manufacturer
Medtech Products Inc.
Effective date
2025-10-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:45:05

Label at a glance#

ProductCompound W Complete Coverage Callus Remover
Active ingredientSALICYLIC ACID
Label structure10 sections

Indications and uses

for the removal of calluses relieves pain by removing calluses 

Dosage and administration

wash affected area and dry thoroughly if necessary, cut medicated patch to fit callus apply medicated patch with sticky side adhering to skin after 48 hours, remove medicated patch repeat procedure every 48 hours as needed for up to 14 days (until callus is removed) may soak callus in warm water for 5 minutes to assist in removal 

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts 

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 40%

Purpose

OTC - PURPOSE SECTION

Callus remover 

Uses

INDICATIONS & USAGE SECTION

  • for the removal of calluses
  • relieves pain by removing calluses 

Warnings

WARNINGS SECTION

For external use only. 

Do not use

OTC - DO NOT USE SECTION

  • if you are a diabetic
  • if you have poor blood circulation
  • on irritated skin or any area that is infected or reddened 

Stop use and ask a doctor if

OTC - STOP USE SECTION

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 and dry thoroughly
  • if necessary, cut medicated patch to fit callus
  • apply medicated patch with sticky side adhering to skin
  • after 48 hours, remove medicated patch
  • repeat procedure every 48 hours as needed for up to 14 days (until callus is removed)
  • may soak callus in warm water for 5 minutes to assist in removal 

Other information

OTHER SAFETY INFORMATION

  • store at room temperature. avoid excessive heat 37ºC(99ºF). 

Inactive ingredients

INACTIVE INGREDIENT SECTION

glyceryl rosinate, lanolin, natural rubber, polyisobutylene, terpene resin, titanium dioxide 

Questions?

OTC - QUESTIONS SECTION

1-800-443-4908 

CompoundW.com 

Dist. by Medtech Products Inc. 

Tarrytown, NY 10591 

A Prestige Consumer Healthcare 

company. ©2025 Trade dress is owned 

by Medtech Products Inc. All rights 

reserved. Made in China.

CWUS046101

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

 

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Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63029-62463029-624-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
GLYCERYL ROSINATESD112V492JIACT
LANOLIN7EV65EAW6HIACT
NATURAL LATEX RUBBER2LQ0UUW8INIACT
POLYISOBUTYLENE (1300 MW)241BN7J12YIACT
TERPENE RESINGR35AH6YDNIACT
TITANIUM DIOXIDE15FIX9V2JPIACT

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
a77da6cb-a95f-4190-8255-9db1e4837a0b6ca9ca00-3f4f-4100-ba75-bb6d4ca756f92026-04-08WarningsExact identifier
spl set id: 6ca9ca00-3f4f-4100-ba75-bb6d4ca756f9

Reported adverse events (FAERS/openFDA)#

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