FUHOP FUNGAL NAIL PATCHES

Manufacturer
Gaozhou Chapin Technology Co., Ltd
Effective date
2024-06-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:14:31

Label at a glance#

ProductFUHOP FUNGAL NAIL PATCHES
Active ingredientTOLNAFTATE
Label structure13 sections

Dosage and administration

Apply this product to the desired nail area, 1-2 times a day. Keep using it. Avoid light, airtight, and store in a cool and dry place.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

TOLNAFTATE 1%

Purpose

OTC - PURPOSE SECTION

bacteriostatic, sterilizing

Use

INDICATIONS & USAGE SECTION

Use for fungal nail infections

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

It is prohibited for those who are allergic to this product and pregnant women, and should be used with caution on open wounds.

When Using

OTC - WHEN USING SECTION

Do not put in eyes,If it accidentally gets into your eyes, rinse with water or seek medical advice.If irritation or rash occurs, discontinue use and ask a doctor. If swallowed, get medical help or contact a Poison Control Center immediately

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs

Ask Doctor

OTC - ASK DOCTOR SECTION

Do not put in eyes,lfit accidentally gets into your eyes, rinse with water or seek medical advice.lfirritation or rash occurs, discontinue use and ask a doctor. if swallowed, get medical help orcontact a Poison Control Centerimmediate.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep this product out of reach of children

DOSAGE & ADMINISTRATION SECTION

One patch per day, each patch contains 1 mg of tolnaftate

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Allantoin,Allium Sativum (Garlic) Bulb Extract,Cnidium,Monnieri Fruit Oil,Melaleuca Alternifolia (Tea Tree) Leaf oil

Directions

RECENT MAJOR CHANGES SECTION

Apply this product to the desired nail area, 1-2 times a day. Keep using it.
Avoid light, airtight, and store in a cool and dry place.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2677690tolnaftate 1 % Medicated PatchPSN2
2677690tolnaftate 0.01 MG/MG Medicated PatchSCD2
2677690tolnaftate 1 % Medicated PatchSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84168-036-012025-07-29C16284748780-13b156c62-2ea2-fb37-e063-e6dba90a4e071bf024c8-666d-3315-e063-6294a90a24f6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84168-036-01FUHOP FUNGAL NAIL PATCHES24 g in 1 BOXPATCH242

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84168-036FUHOP FUNGAL NAIL PATCHES (NAIL RENEW PATCHES) PATCH [GAOZHOU CHAPIN TECHNOLOGY CO., LTD]21 package rows20240701_1bf024c8-666d-3315-e063-6294a90a24f6.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84168-03684168-036-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
1c09cb9c-32b3-db85-e063-6394a90acaa91bf024c8-666d-3315-e063-6294a90a24f62024-06-29WarningsExact identifier
spl id: 1c09cb9c-32b3-db85-e063-6394a90acaa9
spl set id: 1bf024c8-666d-3315-e063-6294a90a24f6

Reported adverse events (FAERS/openFDA)#

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