VTROUY Fungus Nail Renewal

Manufacturer
Guangzhou Qiexiran Cosmetics Co., Ltd.
Effective date
2025-10-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:39:09

Label at a glance#

ProductVTROUY Fungus Nail Renewal
Active ingredientUNDECYLENIC ACID
Label structure14 sections

Dosage and administration

Wash feet thoroughly with warm water, and gently file the thickened part of the fungal nail with a nail file until it's flat. Apply a layer of the liquid to the surface of the fungal nail and allow it to be absorbed into the nail. Repeat the process twice a day. Use it continuously for at least 4 weeks to see the effect. And if you want complete improvement, we recommend using it for 6 weeks or more.

Storage and handling

Store at room temperature and out of direct sunlight. Skin discoloration may occur during or after use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Undecylenic Acid 25%

Purpose

OTC - PURPOSE SECTION

Antifungal

Use

INDICATIONS & USAGE SECTION

Hinder fungal and bacterial growth, reduce itching, cleanse skin tissue.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

On irritated skin and any area that is infected or reddened. If pregnant or if there is any allergic reaction to this product.

When Using

OTC - WHEN USING SECTION

Avoid contact with eyes.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor If discomfort persists.​​

Ask Doctor

OTC - ASK DOCTOR SECTION

If you have diabetes or poor blood circulation.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product gets into eyes, flush with water for 15 minutes.
If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wash feet thoroughly with warm water, and gently file the thickened part of the fungal nail with a nail file until it's flat.
Apply a layer of the liquid to the surface of the fungal nail and allow it to be absorbed into the nail.
Repeat the process twice a day. Use it continuously for at least 4 weeks to see the effect. And if you want complete improvement, we recommend using it for 6 weeks or more.

Other information

STORAGE AND HANDLING SECTION

Store at room temperature and out of direct sunlight.
Skin discoloration may occur during or after use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Mineral oil, Apricot Kernel Oil, Tea Tree Oil, Tocopherol, Peppermint Oil, Camphor Oil, Jojoba Oil, Bergamot Oil, Lavender Oil.

Questions

OTC - QUESTIONS SECTION

Email at cs@vtoury.com​

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
998329undecylenic acid 25 % Topical SolutionPSN1
998329undecylenic acid 250 MG/ML Topical SolutionSCD1
998329undecylenic acid 25 % Topical SolutionSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85817-007-01VTROUY Fungus Nail Renewal2 in 1 BOXLIQUID21
85817-007-01VTROUY Fungus Nail Renewal15 mL in 1 BOTTLELIQUID151

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85817-00785817-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
VTROUY Fungus Nail RenewalFUNGUS NAIL RENEWALGuangzhou Qiexiran Cosmetics Co., Ltd.413f6399-dda1-8dd9-e063-6394a90a573d2025-10-15WarningsExact identifier
ndc (package): 85817-007-01
ndc (product): 85817-007
ndc11 (package): 85817000701
spl id: 413f6399-dda2-8dd9-e063-6394a90a573d
spl set id: 413f6399-dda1-8dd9-e063-6394a90a573d

Reported adverse events (FAERS/openFDA)#

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