DRUGGIST Fungal Nail Renewal

Manufacturer
Shenzhen Xiaomai Manufacturing Co., Ltd.
Effective date
2024-06-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:59:59

Label at a glance#

ProductDRUGGIST Fungal Nail Renewal
Active ingredientUNDECYLENIC ACID, TOLNAFTATE
Label structure13 sections

Dosage and administration

1.Apply the product twice a day, in the morning and at night. 2. For initial use, soak the affected nail in wam water to soften it. Gently file the nail to make it thinner and remove dirt, being cautious not to harm the nail bed. Apply the product after this step. 3. After the first application, repeat every 2-3 days. File the surface of the affected nail and continue regular usage. *In case of ingestion, seek med...

Storage and handling

Please store in a cool, dry place away from direct sunlight.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION


Toinaftate 1%
Undecylenic Acid 25%

​Purpose

OTC - PURPOSE SECTION


-Fungal nails, Athlete's Foot, Tinea Manuum Jock ltch, Ringworm caused by fungus and bacterial infection.

Use

INDICATIONS & USAGE SECTION


-For all caused by nail fungusnail discoloration,nail thickening,nail splitting,nail crumbling.

Warnings

WARNINGS SECTION


* For external use only, do not ingest.
* Avoid eye contact; maintain dry andclean skin.
* Exercise caution when using on severelyulcerated skin.
* Keep out of reach of children.
* This product is not a substitute formedication.

Do not use

OTC - DO NOT USE SECTION

* For external use only, do not ingest.

When Using

OTC - WHEN USING SECTION

* Avoid eye contact; maintain dry andclean skin.
* Exercise caution when using on severelyulcerated skin.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

Ask Doctor

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if rash occurs

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

1.Apply the product twice a day, in the morning and at night.
2. For initial use, soak the affected nail in wam water to soften it. Gently file the nail to make it thinner and remove dirt, being cautious not to harm the nail bed. Apply the product after this step.
3. After the first application, repeat every 2-3 days. File the surface of the affected nail and continue regular usage.
*In case of ingestion, seek medical assistance or contact a poison control center immediately.

Other information

STORAGE AND HANDLING SECTION

Please store in a cool, dry place away from direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION


Ethyl Lactate, Aqua,Lactic Acid,Resacetophenone,Acetic Acid, Sophora Flavescens Extract,Stellera Chamaejasme Leaf/Stem Extract,Crocus Sativus Style Extract,Eucalyptol,Olive Oil,Lavender,Aloe Barbadensis Leaf Extract, Carthamus Tinctorius (Safflower) Seed Oil, Hydrogenated Polyisobutene,Lavandula Angustifolia (Lavender) Oil,Melaleuca Alternifolia (Tea Tree) Leaf Oil, Oryza Sativa (Rice) Bran Oil,Prunus Amygdalus Dulcis (Sweet Almond) Oil,Sesamum indicum (Sesame) Seed Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Tocopheryl Acetate.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83872-262DRUGGIST FUNGAL NAIL RENEWAL (FUNGAL NAIL RENEWAL) LIQUID [SHENZHEN XIAOMAI MANUFACTURING CO., LTD.]1Unmatched20240628_1bccb874-2cde-21bd-e063-6394a90a512f.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83872-26283872-262-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
36574cb1-1cfc-c8df-e063-6294a90a6cb61bccb874-2cde-21bd-e063-6394a90a512f2025-05-30WarningsExact identifier
spl set id: 1bccb874-2cde-21bd-e063-6394a90a512f

Reported adverse events (FAERS/openFDA)#

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