DRUGGIST FUNGI NALL

Manufacturer
Shenzhen Xiaomai Manufacturing Co., Ltd.
Effective date
2024-06-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:59:54

Label at a glance#

ProductDRUGGIST FUNGI NALL
Active ingredientTOLNAFTATE, UNDECYLENIC ACID
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.

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

Undecylenic Acid

Purpose

OTC - PURPOSE SECTION

-Fungal nails, Athlete's Foot, Tinea Manuum Jock ltch, Ringworm caused by fungus and bacterial infection.
-For all caused by nail fungusnail discoloration,nail thickening,nail splitting,nail crumbling.

Use

INDICATIONS & USAGE SECTION

-Fungal nails, Athlete's Foot, Tinea Manuum Jock ltch, Ringworm caused by fungus and bacterial infection.
-For all caused by nail fungusnail discoloration,nail thickening,nail splitting,nail crumbling.

Warnings

WARNINGS 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.

Do not use

OTC - DO NOT USE SECTION

* For external use only, do not ingest.

* Exercise caution when using on severelyulcerated skin.

When Using

OTC - WHEN USING SECTION

* Avoid eye contact; maintain dry andclean skin.

Stop Use

OTC - STOP USE SECTION

Keep out of reach of children.

Ask Doctor

OTC - ASK DOCTOR SECTION


Exercise caution when using on severelyulcerated skin.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out Of Reach Of Chlidren

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.

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LBEALLBEAL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83872-263DRUGGIST FUNGI NALL (FUNGI NALL) LIQUID [SHENZHEN XIAOMAI MANUFACTURING CO., LTD.]1Unmatched20240630_1bf14bc1-b288-5e2c-e063-6394a90a2296.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83872-26383872-263-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
3657406d-3fa2-bec9-e063-6394a90ac71c1bf14bc1-b288-5e2c-e063-6394a90a22962025-05-30WarningsExact identifier
spl set id: 1bf14bc1-b288-5e2c-e063-6394a90a2296

Reported adverse events (FAERS/openFDA)#

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