Nekvnro Wart remover patch

Manufacturer: Shenzhen Xingqi Technology Co., Ltd.
Effective date: 2024-08-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:16:56

Label at a glance#

ProductNekvnro Wart remover patch

Active ingredientTALC

Label structure11 sections

Indications and uses

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

Dosage and administration

For external use only.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

TALC 1%

PURPOSE

OTC - PURPOSE SECTION

wart removal

USES

INDICATIONS & USAGE SECTION

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

warning

WARNINGS SECTION

1, external use,Avoid contact with eyes and mouth.
2,If irritation or abnormality occurs, stop using and wash with water
3, Please keep this product out of the reach of children

Dosage and administration

DOSAGE & ADMINISTRATION SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

1, external use, Avoid contact with eyes and mouth.
2,lf irritation or abnormality occurs, stop using and wash with water
3, Please keep this product out of the reach of children

When using section

OTC - WHEN USING SECTION

1, external use,Avoid contact with eyes and mouth.
2,lf irritation or abnormality occurs, stop using and wash with water
3, Please keep this product out of the reach of children

STOP USE

OTC - STOP USE SECTION

1, external use, Avoid contact with eyes and mouth.
2,lf irritation or abnormality occurs, stop using and wash with water
3, Please keep this product out of the reach of children

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep this product out of the reach of children

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

POTASSIUM ALUM , SODIUM ALGINATE

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
84613-052-01	2025-07-29	C162847	48780-1	3b156c62-2bea-fb37-e063-e6dba90a4e07	1f2e447e-7407-5f48-e063-6294a90ad66c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84613-052-01	Nekvnro Wart remover patch	30 g in 1 BOX	PATCH	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84613-052	NEKVNRO WART REMOVER PATCH (WART REMOVER PATCH) PATCH [SHENZHEN XINGQI TECHNOLOGY CO., LTD.]	1	1 package rows	20240809_1f2e447e-7407-5f48-e063-6294a90ad66c.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Nekvnro Wart remover patch
Wart remover patch
POTASSIUM ALUM
SODIUM ALGINATE
TALC

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84613-052	84613-052-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
POTASSIUM ALUM	1L24V9R23S	IACT
SODIUM ALGINATE	C269C4G2ZQ	IACT
TALC	7SEV7J4R1U	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
1f2e447e-7408-5f48-e063-6294a90ad66c			1f2e447e-7407-5f48-e063-6294a90ad66c	2024-08-08	Warnings	Exact identifier spl id: 1f2e447e-7408-5f48-e063-6294a90ad66c spl set id: 1f2e447e-7407-5f48-e063-6294a90ad66c

Reported adverse events (FAERS/openFDA)#

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