Compound W Complete Coverage Callus Remover 63029-624-08

Compound W Complete Coverage Callus Remover by

Drug Labeling and Warnings

Compound W Complete Coverage Callus Remover by is a Otc medication manufactured, distributed, or labeled by Medtech Products Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

COMPOUND W COMPLETE COVERAGE CALLUS REMOVER- salicylic acid plaster 
Medtech Products Inc.

----------

Compound W Complete Coverage Callus Remover 63029-624-08

Drug Facts 

Active ingredient

Salicylic acid 40%

Purpose

Callus remover 

Uses

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

Warnings

For external use only. 

Do not use

• 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

discomfort persists. 

Keep out of reach of children.

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

Directions

• 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

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

Inactive ingredients

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

Questions?

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

 

COMPOUND W COMPLETE COVERAGE CALLUS REMOVER 
salicylic acid plaster

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63029-624
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.4 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERYL ROSINATE (UNII: SD112V492J)
LANOLIN (UNII: 7EV65EAW6H)
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
POLYISOBUTYLENE (1300 MW) (UNII: 241BN7J12Y)
TERPENE RESIN (UNII: GR35AH6YDN)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63029-624-08	8 in 1 CARTON; Type 0: Not a Combination Product	12/01/2025	04/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M030	12/01/2025	04/01/2026

Labeler - Medtech Products Inc. (122715688)

Revised: 4/2026

Document Id: a77da6cb-a95f-4190-8255-9db1e4837a0b

34390-5

Set id: 6ca9ca00-3f4f-4100-ba75-bb6d4ca756f9

Version: 3

Effective Time: 20260408