FDA.reportPublic FDA data

Topcare Liquid Wart Remover

Manufacturer
Topco Associates LLC
Effective date
2026-09-25
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
daily-update
Hydrated at
2026-09-29 01:03:34

Label at a glance#

ProductSalicylic Acid
Active ingredientSALICYLIC ACID
Label structure9 sections

Dosage and administration

wash affected area, may soak wart in warm water for 5 minutes dry area thoroughly apply small amount of wart remover with applicator to sufficiently cover each wart let dry and repeat this procedure once or twice daily until wart is removed for up to 12 weeks

Label contents#

Full prescribing information#

​Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 17%w/w

Purpose

OTC - PURPOSE SECTION

Wart Remover

Use

INDICATIONS & USAGE SECTION

  • for the removal of common and plantar warts. The common
    wart is easily recognized by the rough 'cauliflower-like' appearance of
    the surface. Plantar wart is recognized by its location only on the bottom
    of the foot, its tendemess and the interruption of the footprint pattern.

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 heat

Do not use

OTC - DO NOT USE SECTION

  • if you are diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist
  • genital warts and warts on the face
  • on moles, birthmarks and warts with hair growing from them
  • on mucous membranes
  • on irritated, infected or reddened skin

​When using this product

OTC - WHEN USING SECTION

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

Stop use and ask 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 affected area, may soak wart in warm water for 5 minutes
  • dry area thoroughly
  • apply small amount of wart remover with applicator to sufficiently cover each wart
  • let dry and repeat this procedure once or twice daily until wart is removed for up to 12 weeks

Other information

OTHER SAFETY INFORMATION

  • store between 20°-25°℃ (68°-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

MAXIMUM STRENGTH

Liquid

Wart

Remover

SALICYLIC ACID 17%

  • Removes Common

& Plantar Warts

  • Convenient Brush Applicator
  • Safe & Effective

NET 0.31 FL OZ (9 mL)

liquid wart removerliquid wart remover

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codetopbrnds.com/48zrpgTop Care_Liquid Wart Remover_53-012TC-02.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
36800-376-092023-01-31C16284748780-1f386c649-f4c7-0266-e053-dadaa90a7c1aTopcare Liquid Wart Remover
36800-376-092023-01-31C16284748780-1f386c649-f4c7-0266-e053-dadaa90a7c1aTopcare Liquid Wart Remover
36800-376-092023-01-31C16284748780-1f386c649-f4c7-0266-e053-dadaa90a7c1aTopcare Liquid Wart Remover

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
36800-37636800-376-09

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
72025-10-07full-release2026-06-01 01:38:09
62024-12-11full-release2026-06-01 00:42:28

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
40979d8f-eac7-62b2-e063-6294a90ab5dc78beaf1b-14a2-45f9-ad0d-0d8953d316b32025-10-07WarningsExact identifier
spl set id: 78beaf1b-14a2-45f9-ad0d-0d8953d316b3

Reported adverse events (FAERS/openFDA)#

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