CORN REMOVER

Manufacturer
Shenzhen Hengdasheng Technology Co., Ltd
Effective date
2026-01-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:33:36

Label at a glance#

ProductCORN REMOVER
Active ingredientSALICYLIC ACID
Label structure12 sections

Dosage and administration

1. Wash the affected area and dry thoroughly. 2. Place firmly the medicated round part over the center of corn, adhesive next to skin.(If necessary, cut the medicated patch to fit corn.) 3. Leave in place for up to24 hours. 4. Replace with a new pad every24 hours. 5. May soak corn in warm water for 5 minutes to assist in the remova. 6. Repeat daily as needed until the corn is removed. 7. Do not use for more than 1...

Storage and handling

Store between 15° and 30°C(59° and 86°F) Protect from excessive heat and temperaturesabove 40°C(140°F).

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 40%

Purpose

OTC - PURPOSE SECTION

Corn Remover

Use

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 have poor blood circulation

if you are diabetic, pregnant or breastfeeding

On irritated skin or on any area that is infected or reddened.

OTC - WHEN USING SECTION

Do not use with other topical products on the same area unless directed by a doctor.

OTC - STOP USE SECTION

Stop use and ask a doctor if discomfort lasts

If discomfort persists see your doctor or podiatrist Keep out of reach of children.

If swallowed,get medical help or contact a Poison Control Center right away

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

1. Wash the affected area and dry thoroughly.

2. Place firmly the medicated round part over the center of corn, adhesive next to skin.(If necessary, cut the medicated patch to fit corn.)

3. Leave in place for up to24 hours.

4. Replace with a new pad every24 hours.

5. May soak corn in warm water for 5 minutes to assist in the remova.

6. Repeat daily as needed until the corn is removed.

7. Do not use for more than 14 days for corns unless directed by a doctor.

Other information

STORAGE AND HANDLING SECTION

Store between 15° and 30°C(59° and 86°F)

Protect from excessive heat and temperaturesabove 40°C(140°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Phenol, White Petrolatum, Lanolin, Paraffinum Liquidum

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
240559salicylic acid 40 % Medicated PatchPSN2
240559salicylic acid 0.4 MG/MG Medicated PatchSCD2
240559salicylic acid 40 % Medicated PatchSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87308-002-01CORN REMOVER42 U in 1 BOXPATCH422

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87308-00287308-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
CORN REMOVERCORN REMOVERShenzhen Hengdasheng Technology Co., Ltd47f36a54-a1f2-e96e-e063-6294a90a90692026-01-17WarningsExact identifier
ndc (package): 87308-002-01
ndc (product): 87308-002
ndc11 (package): 87308000201
spl id: 488f7bb1-95e5-e63a-e063-6394a90a860c
spl set id: 47f36a54-a1f2-e96e-e063-6294a90a9069

Reported adverse events (FAERS/openFDA)#

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