Nekvnro Wart Remover Patch

Manufacturer
Guoyu Trading Co., Ltd.
Effective date
2024-10-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:30:10

Label at a glance#

ProductNekvnro Wart Remover Patch
Active ingredientSALICYLIC ACID
Label structure12 sections

Dosage and administration

lean and wipe the skin around the wart,Remove the wart removal tablet.Apply it to the wart,Cover it completely,1capsule can last for 8-12 hours, Recommended 2-3 times a day.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 1%

Purpose

OTC - PURPOSE SECTION

Anti-inflammatory and analgesic

Use

INDICATIONS & USAGE SECTION

Wart removal patch can reduce inflammation, relieve pain and soften cuticles.

Warnings

WARNINGS SECTION

external use,Avoid contact with eyes and mouth.

Do not use

OTC - DO NOT USE SECTION

if irritation or abnormality occurs, stop using and wash with water.

When Using

OTC - WHEN USING SECTION

Avoid contact with eyes and mouth,if irritation or abnormality occurs, stop using and wash with water,Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Stop Use

OTC - STOP USE SECTION

Avoid contact with eyes and mouth,if irritation or abnormality occurs, stop using and wash with water.

Ask Doctor

OTC - ASK DOCTOR SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Keep Oot 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

lean and wipe the skin around the wart,Remove the wart removal tablet.Apply it to the wart,Cover it completely,1capsule can last for 8-12 hours, Recommended 2-3 times a day.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Hydrocolloid,Cellulose Gum,Polyisobutylene,Polyisobutylene,Cyperus rotundus,Prunella vulgaris.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122334455667788991010

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2688025salicylic acid 1 % Medicated PatchPSN1
2688025salicylic acid 0.01 MG/MG Medicated PatchSCD1
2688025salicylic acid 1 % Medicated PatchSY1

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
84844-002-012026-01-29C16284748780-149896155-cc11-586f-e063-e6dba90add9084844-002
84844-002-022026-01-29C16284748780-149896155-cc11-586f-e063-e6dba90add9084844-002

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84844-002-01Nekvnro Wart Remover Patch216 in 1 BOXPATCH2161
84844-002-02Nekvnro Wart Remover Patch360 in 1 BOXPATCH3601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84844-002NEKVNRO WART REMOVER PATCH (WART REMOVER PATCH) PATCH [GUOYU TRADING CO., LTD.]12 package rows20241029_2521c88a-571f-4e3e-e063-6394a90ac78e.zip

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
84844-00284844-002-01, 84844-002-02

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
2521c88a-5720-4e3e-e063-6394a90ac78e2521c88a-571f-4e3e-e063-6394a90ac78e2024-10-23WarningsExact identifier
spl id: 2521c88a-5720-4e3e-e063-6394a90ac78e
spl set id: 2521c88a-571f-4e3e-e063-6394a90ac78e

Reported adverse events (FAERS/openFDA)#

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