HEB Gel Corn Remover

Manufacturer: HEB
Effective date: 2026-05-27
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:58:56

Label at a glance#

ProductGel Corn Remover

Active ingredientSALICYLIC ACID

Label structure9 sections

Indications and uses

for the removal of corns relieves pain by removing corns

Dosage and administration

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

Contacts and useful links#

PhoneLabel contact1-866-964-0939

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 40%

Purpose

OTC - PURPOSE SECTION

Corn remover

Uses

INDICATIONS & USAGE SECTION

for the removal of corns
relieves pain by removing corns

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 on any area that is infected or reddened

Stop use and ask a doctor if

OTC - ASK DOCTOR 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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

OTHER SAFETY INFORMATION

store between 15° and 30°C (59° and 86°F)
avoid surrounding skin when applying medicated disc

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

Questions?

OTC - QUESTIONS SECTION

call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.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

carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
240559	salicylic acid 40 % Medicated Patch	PSN	1
240559	salicylic acid 0.4 MG/MG Medicated Patch	SCD	1
240559	salicylic acid 40 % Medicated Patch	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59640-802-01	Gel Corn Remover	6 in 1 BOX	PATCH	6		1
59640-802-01	Gel Corn Remover	1 g in 1 PATCH	PATCH	1		1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Gel Corn Remover
Salicylic Acid
HIGH DENSITY POLYETHYLENE
POLYVINYL ALCOHOL, UNSPECIFIED

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59640-802	59640-802-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
HIGH DENSITY POLYETHYLENE	UG00KM4WR7	IACT
SALICYLIC ACID	O414PZ4LPZ	ACTIB
POLYVINYL ALCOHOL, UNSPECIFIED	532B59J990	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Gel Corn Remover	SALICYLIC ACID	HEB	52d0c9e5-b943-7459-e063-6294a90a35f2	2026-05-27	Warnings	Exact identifier ndc (package): 59640-802-01 ndc (product): 59640-802 ndc11 (package): 59640080201 spl id: 52d0b0de-ec81-1be8-e063-6394a90a3591 spl set id: 52d0c9e5-b943-7459-e063-6294a90a35f2

Reported adverse events (FAERS/openFDA)#

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