GNP Liquid Corn & Callus Remover

Manufacturer
AmerisourceBergen Drug Corporation
Effective date
2026-08-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-07 01:01:32

Label at a glance#

ProductLiquid Corn and Callus
Active ingredientSALICYLIC ACID
Label structure9 sections

Indications and uses

for the removal of corns and calluses relieves pain by removing corns and calluses

Dosage and administration

wash the affected area and dry thoroughly apply one drop at a time with applicator to sufficiently cover each corn/callus let dry use cushion with hole centered over corn or callus to relieve pressure (additional cushions may be purchased separately) hold cushion down 2-3 seconds to adhere to skin repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed) may soak corn/cal...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 17%w/w

Purpose

OTC - PURPOSE SECTION

Corn and callus remover

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

Flammable

SAFE HANDLING WARNING SECTION

  • keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

  • on irritated skin
  • on any area that is infected or reddened
  • if you are a diabetic, or if you have poor blood circulation

When using this product

OTC - WHEN USING SECTION

  • if product gets into the eyes, flush with water for 15 minutes
  • avoid inhaling vapors
  • cap bottle tightly and store at room temperature away from heat

Stop use and ask a doctor if

OTC - STOP USE 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 the affected area and dry thoroughly
  • apply one drop at a time with applicator to sufficiently cover each corn/callus
  • let dry
  • use cushion with hole centered over corn or callus to relieve pressure (additional cushions may be purchased separately)
  • hold cushion down 2-3 seconds to adhere to skin
  • repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)
  • may soak corn/callus in warm water for 5 minutes to assist in removal

Other information

OTHER SAFETY INFORMATION

  • store between 20° - 25°C (68° - 77°F)
  • avoid surrounding skin when applying product
  • close tightly to prevent solidification
  • wipe top of bottle clean after each use
  • do not allow to come into contact with fabrics, floors, countertops or other surfaces--will stain

Inactive ingredients

INACTIVE INGREDIENT SECTION

camphor, castor oil, ethanol, ethyl ether, nitrocellulose

Questions?

OTC - QUESTIONS SECTION

Call 1-888-287-1915

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GOOD
NEIGHBOR
PHARMACY

Liquid Corn &
Callus Remover

Salicylic Acid 17%/ Corn & Callus Remover

  • Safely removes corns & calluses
  • Soft foam cushions & protects

3 Cushions
0.33 FL. OZ. (9.8 mL)

cartoncarton

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
46122-83846122-838-72

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
Liquid Corn and CallusSALICYLIC ACIDAmerisourceBergen Drug Corporation583fd150-44c8-b4e4-e063-6294a90af9592026-08-04WarningsExact identifier
ndc (package): 46122-838-72
ndc (product): 46122-838
ndc11 (package): 46122083872
spl id: 583fd157-d894-c2fc-e063-6394a90a6258
spl set id: 583fd150-44c8-b4e4-e063-6294a90af959

Reported adverse events (FAERS/openFDA)#

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