FDA.reportPublic FDA data

Fungal Nail Treatment

Manufacturer
Guangzhou Yixin Cross-border E-commerce Co., Ltd.
Effective date
2025-07-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:06:11

Label at a glance#

ProductFungal Nail Treatment
Active ingredientEUCALYPTUS GLOBULUS WHOLE
Label structure11 sections

Indications and uses

For the effective treatment of nail fungus, discoloration, thickening, splitting, crumbling and brittleness

Dosage and administration

For initial use, soak the affected nail in warm water to soften it. Gently fle thenail to make it thinner and remove dirt, being cautiousnot to harm the nail bed. Apply full layers of nail solution with brush onto affected areas on, around, and under nails. A light tingle or burn is normal for the first 10 minutes until the product is absorbed into the skin. Apply the product twice a day, in the morning and at nig...

Label contents#

Full prescribing information#

Active ingredients

COMPONENTS

Eucalyptus Globulus Whole 1%

Purpose

OTC - PURPOSE SECTION

Anti-funga

Uses

INDICATIONS & USAGE SECTION

For the effective treatment of nail fungus, discoloration, thickening, splitting, crumbling and brittleness

Warnings

WARNINGS SECTION

For external use only.

Dosage and administration

DOSAGE & ADMINISTRATION SECTION

For initial use, soak the affected nail in warm water to soften it. Gently fle thenail to make it thinner and remove dirt, being cautiousnot to harm the nail bed.

Apply full layers of nail solution with brush onto affected areas on, around, and under nails. A light tingle or burn is normal for the first 10 minutes until the product is absorbed into the skin.

Apply the product twice a day, in the morning and at night.

Visible results will be seen in as little as 7 days, continue regular usage to prevent fungus regrowth.

Do not use

OTC - DO NOT USE SECTION

Children under 2 years of age

pregnant or if there is any allergic reaction to this produce

When using section

OTC - WHEN USING SECTION

Avoid contact with eyes

stop use

OTC - STOP USE SECTION

lrritation occurs or discomfort persists

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

lf product gets into eyes, flush with water for 15 minutes.

lf swallowed, get medical help or contact a Poison Control Center right away.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Peppermint oil, SAFFLOWER OIL, NOTOGINSENG RADIX

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

222222222222222222

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84778-075-01Fungal Nail Treatment15 g in 1 BOTTLELIQUID153

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
84778-07584778-075-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
PEPPERMINT OILAV092KU4JHIACT
EUCALYPTUS GLOBULUS WHOLESI1P2XF3M3ACTIM
PANAX NOTOGINSENG ROOTGQX1C1175UIACT
SAFFLOWER OIL65UEH262ISIACT

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
38d9d0c2-f102-a001-e063-6394a90a9dd5378b3f1b-80bb-0e63-e063-6394a90a82972025-07-01WarningsExact identifier
spl id: 38d9d0c2-f102-a001-e063-6394a90a9dd5
spl set id: 378b3f1b-80bb-0e63-e063-6394a90a8297

Reported adverse events (FAERS/openFDA)#

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