SottSunFeli Wart Remover

Manufacturer
Henan Toudaorong Biotechnology Co., Ltd.
Effective date
2025-11-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:16:05

Label at a glance#

ProductSottSunFeli Wart Remover
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

SALICYLIC ACID

OTC - PURPOSE SECTION

for the removal of common and plantar warts

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of chlldren

WARNINGS SECTION

For external use only. Flammable.
Keep away from fire and flame.

INDICATIONS & USAGE SECTION

Wash the affected area.
May soak wart in warm water for 5 minutes.

Dry area thoroughly.

Use a brush to apply a sufficient amount to cover each wart. Let it dry.

Repeat this procedure once or twice daily as needed (until wart is removed) for up to 12 weeks.

DOSAGE & ADMINISTRATION SECTION

Wash the affected area.
May soak wart in warm water for 5 minutes.

INACTIVE INGREDIENT SECTION

BORNEOL

POLYETHYLENE GLYCOL, UNSPECIFIED

WATER

GLYCERIN

PODOFILOX

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
238466salicylic acid 15 % Topical SolutionPSN1
238466salicylic acid 150 MG/ML Topical SolutionSCD1
238466salicylic acid 15 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a90fd6c4-df39-45aa-ddf9-e6c34fff3951Product name220250805
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
22fe7b8d-6b80-a6ee-3b72-558f5763c606Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85136-010-01SottSunFeli Wart Remover20 mL in 1 BOTTLELIQUID201

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
85136-01085136-010-01

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
438bde30-3e25-9157-e063-6294a90a1423438bde30-3e24-9157-e063-6294a90a14232025-11-14WarningsExact identifier
spl id: 438bde30-3e25-9157-e063-6294a90a1423
spl set id: 438bde30-3e24-9157-e063-6294a90a1423

Reported adverse events (FAERS/openFDA)#

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