Nekvnro Freckle Removal Patch

Manufacturer
Shenzhen Xingqi Technology Co., Ltd.
Effective date
2024-10-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:24:11

Label at a glance#

ProductNekvnro Freckle Removal Patch
Active ingredientNIACINAMIDE, ARBUTIN
Label structure11 sections

Indications and uses

Usage Method 1.Clean and dry the application area thoroughly. 2. Remove the patch from the protective film, Then apply the patch to the affected area. 3. Gently press the edges of the patch for better adhesion. 4.Each patch can be used for 8-12 hours, Change at least 2-3 times a day.

Dosage and administration

For external use only.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Niacinamide 1%

Arbutin 1%

Purpose

OTC - PURPOSE SECTION

Freckle Removal Patch

Uses

INDICATIONS & USAGE SECTION

Usage Method
1.Clean and dry the application area thoroughly.
2. Remove the patch from the protective film, Then apply the patch to the affected area.
3. Gently press the edges of the patch for better adhesion.
4.Each patch can be used for 8-12 hours, Change at least 2-3 times a day.

Warnings

WARNINGS SECTION

Precautions
1. external use, Avoid contact with eyes and mouth.
2. Stop using if you feel irritation or abnormality, Wash with water.
3. Keep this product out of reach ofchildren.

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,Stop using if you feel irritation or abnormality,Wash with water.
3,Keep this product out of reach of children.

When using section

OTC - WHEN USING SECTION

1,external use, Avoid contact with eyes and mouth.
2,Stop using if you feel irritation or abnormality,Wash with water.
3,Keep this product out of reach of children.

stop use

OTC - STOP USE SECTION

1, external use,Avoid contact with eyes and mouth.
2,Stop using if you feel irritation or abnormality,Wash with water.
3, Keep this product out of reach of children.

KEEP OUT OF REACH OF CHILDREN SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this product out of reach of children.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Hydrocolloid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABELLABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84613-059-012025-07-29C16284748780-13b156c62-2666-fb37-e063-e6dba90a4e072426f72f-75dc-23c9-e063-6294a90af71a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84613-059-01Nekvnro Freckle Removal Patch50 g in 1 BOXPATCH501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84613-059NEKVNRO FRECKLE REMOVAL PATCH (FRECKLE REMOVAL PATCH) PATCH [SHENZHEN XINGQI TECHNOLOGY CO., LTD.]11 package rows20241012_2426f72f-75dc-23c9-e063-6294a90af71a.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84613-05984613-059-01

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
NameUNIIKind
SODIUM ALGINATEC269C4G2ZQIACT
NIACINAMIDE25X51I8RD4ACTIB
ARBUTINC5INA23HXFACTIB

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
2426f72f-75dd-23c9-e063-6294a90af71a2426f72f-75dc-23c9-e063-6294a90af71a2024-10-10WarningsExact identifier
spl id: 2426f72f-75dd-23c9-e063-6294a90af71a
spl set id: 2426f72f-75dc-23c9-e063-6294a90af71a

Reported adverse events (FAERS/openFDA)#

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