Wart Remover

Manufacturer
Shenzhen Bullfighting Trading Co., Ltd.
Effective date
2025-06-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:06:00

Label at a glance#

ProductWart Remover
Active ingredientSALICYLIC ACID
Label structure14 sections

Dosage and administration

*Wash the affected area.*Dry thoroughly.* Use a cotton swab to apply a sufficient amount to cover each wart. Let it dry. Apply twice daily (2-3 applications per use). Use daily for 5-7 days.

Storage and handling

Avoid prolonged exposure to air, as the liquidcan easily volatilize and crystallize. Tighten thecap after each use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 17%

Purpose

OTC - PURPOSE SECTION

Wart Remover

Use

INDICATIONS & USAGE SECTION

For the removal of common warts and plantarwarts. Common warts have a rough, "cauliflowwer-like" surface, making them easy to identify.Plantar warts appear only on the soles of thefeet, are tender to the touch, and disrupt thenatural skin line pattern.

Warnings

WARNINGS SECTION

Avoid contact with eyes, mouth, and open wounds. Rinse immediately if accidental exposure occurs. If irritation persists, seek
medical attention immediately.
• Keep out of reach of children and pets.

Do not use

OTC - DO NOT USE SECTION

On damaged skin (cuts, abrasions, eczema, sunburn).
If you have diabetes or poor blood circulation.

When Using

OTC - WHEN USING SECTION

Skin discoloration may occur during or after use.

Stop Use

OTC - STOP USE SECTION

if irritation occurs. if an allergic reaction occurs.

Ask Doctor

OTC - ASK DOCTOR SECTION

if you are pregnant or breastfeeding.
if you have diabetes

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets.

If swallowed, get medical help or contact a Poison Control Center immediately (1-800-222-1222).
Children should use under adult supervision.

Directions

DOSAGE & ADMINISTRATION SECTION

*Wash the affected area.*Dry thoroughly.*
Use a cotton swab to apply a sufficient amount to cover each wart. Let it dry.
Apply twice daily (2-3 applications per use).
Use daily for 5-7 days.

Other information

STORAGE AND HANDLING SECTION

Avoid prolonged exposure to air, as the liquidcan easily volatilize and crystallize. Tighten thecap after each use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,Polyethylene Glycol,Glycerin,Borneol,Podofilox

Questions

OTC - QUESTIONS SECTION

Email:douniu1@outlook.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312881salicylic acid 17 % Topical SolutionPSN1
312881salicylic acid 170 MG/ML Topical SolutionSCD1
312881salicylic acid 17 % 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
85834-002-01Wart Remover30 mL in 1 BOTTLELIQUID301

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85834-00285834-002-01

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
38c2422d-65de-ca83-e063-6294a90a5e2d38c2422d-65dd-ca83-e063-6294a90a5e2d2025-06-29WarningsExact identifier
spl id: 38c2422d-65de-ca83-e063-6294a90a5e2d
spl set id: 38c2422d-65dd-ca83-e063-6294a90a5e2d

Reported adverse events (FAERS/openFDA)#

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