GEL CORN REMOVER- salicylic acid patch

Drug Labeling and Warnings

Drug Details [pdf]

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 on 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 right away.

Directions

• wash affected area and dry thoroughly
• carefully apply adhesive side of medicated disc onto corn
• cover medicated disc with gel cushion
• after 48 hours remove the medicated disc
• repeat this 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 between 15° and 30°C (59° and 86°F)
• avoid surrounding skin when applying medicated disc

Inactive ingredients

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

Questions?

call 1-866-964-0939

Principal Display Panel

HEB

MAXIMUM STRENGTH
MEDICATED
CLEAR GEL
CORN
REMOVERS

SALICYLIC ACID 40% / CORN REMOVER

• EFFECTIVE CORN REMOVAL TREATMENT
• THIN, FLEXIBLE BANDAGE CONCEALS & PROTECTS
• CLEAR GEL CUSHIONS AFFECTED AREA

6 CUSHIONS

6 MEDICATED DISCS

INGREDIENTS AND APPEARANCE

GEL CORN REMOVER 
salicylic acid patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59640-802
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	400 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59640-802-01	6 in 1 BOX	05/21/2026
1		1 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M030	05/21/2026

Labeler - HEB (007924756)