FDA.reportPublic FDA data

Topco Liquid Corn and Callus Remover

Manufacturer
Topco Associates LLC
Effective date
2026-09-24
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
daily-update
Hydrated at
2026-09-26 01:01:25

Label at a glance#

ProductSalicylic Acid
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) repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)

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
  • cap bottle tightly and store at room temperature away from heat

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, except under the advice and supervision of a doctor or podiatrist

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes
  • avoid inhaling vapors
  • if product gets into the eyes, flush with water for 15 minutes

Stop and ask a doctor if

OTC - STOP USE SECTION

If discomfort persists, see your doctor or podiatrist

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)
  • repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)

Other information

OTHER SAFETY INFORMATION

  • store between 20°C - 25°C (68°F to 77°F)
  • close tightly to prevent solidification
  • store in a cool place

Inactive ingredients

INACTIVE INGREDIENT SECTION

camphor, castor oil, ethanol, ethyl ether, nitrocellulose

Questions?

OTC - QUESTIONS SECTION

Call 1-888-423-0139

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Topcare health

Liquid Corn & Callus Remover
SALICYLIC ACID 17%

  • Safely Removes Corns and Calluses
  • Soft Foam Cushions & Protects



3 CUSHIONS

0.33 FL OZ (9.8mL)

LCCRLCCR

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codetopbrnds.com/48zrm3Top Care_LCCR_41-030TC-02.jpg

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
36800-005-092023-01-31C16284748780-1f386c649-ba78-0266-e053-dadaa90a7c1aTopco Liquid Corn and Callus Remover
36800-005-092023-01-31C16284748780-1f386c649-ba78-0266-e053-dadaa90a7c1aTopco Liquid Corn and Callus Remover
36800-005-092023-01-31C16284748780-1f386c649-ba78-0266-e053-dadaa90a7c1aTopco Liquid Corn and Callus Remover

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZ1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ1
CAMPHOR (NATURAL)INACTIVE INGREDIENTN20HL7Q9411
CASTOR OILINACTIVE INGREDIENTD5340Y2I9G1
PYROXYLININACTIVE INGREDIENTKYR8BR2X6O1

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
36800-00536800-005-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
NITROCELLULOSEKYR8BR2X6OIACT
CAMPHOR (NATURAL)N20HL7Q941IACT
CASTOR OILD5340Y2I9GIACT
ALCOHOL3K9958V90MIACT
ETHYL ETHER0F5N573A2YIACT

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
102025-10-08full-release2026-06-01 01:38:14
92024-12-11full-release2026-06-01 00:42:11

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
CASTOR OILCASTOR OILD5340Y2I9GOINTMENT / TOPICAL14.9 %w/wExact identifier — unii+route
4 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GOINTMENT / TOPICAL14.9 %w/wExact identifier — unii+route
4 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GSOLUTION / TOPICAL1.38 %w/wExact identifier — unii+route
4 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GSOLUTION / TOPICAL1.38 %w/wExact identifier — unii+route
4 equally ranked IID candidates

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
40abc8c8-213c-530f-e063-6294a90af67602755d5c-76c4-4bc8-aaee-d9a17d3958952025-10-08WarningsExact identifier
spl set id: 02755d5c-76c4-4bc8-aaee-d9a17d395895

Reported adverse events (FAERS/openFDA)#

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