COMPOUND W ONE STEP MEDICATED CORN REMOVER- salicylic acid plaster

Compound W One Step Medicated Corn Remover by

Drug Labeling and Warnings

Compound W One Step Medicated Corn Remover by is a Otc medication manufactured, distributed, or labeled by Medtech Products Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts 

Active ingredient 

Salicylic acid 40%

Purpose

Corn remover 

Uses

for the removal of corns relieves pain by removing corns 

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 apply medicated bandage 

after 48 hours, remove medicated bandage repeat procedure every 48 hours as 

needed for up to 14 days (until corn is removed) may soak corn in warm water for 

5 minutes to assist in removal 

Other information  

• store at room temperature 
  
• avoid excessive heat 37°C (99°F) 

Inactive ingredients:

glyceryl rosinate, lanolin, natural rubber, polyisobutylene 

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. 
CWUS038101 

Principal Display Panel

Compound W
CORN REMOVER
Salicylic acid
ONE STEP MEDICATED
CORN REMOVER
8 MEDICATED BANDAGES

INGREDIENTS AND APPEARANCE

COMPOUND W ONE STEP MEDICATED CORN REMOVER 
salicylic acid plaster

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63029-621
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63029-621-08	8 in 1 CARTON; Type 0: Not a Combination Product	12/01/2025

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

Labeler - Medtech Products Inc. (122715688)