FDA.reportPublic FDA data

FUHOP NAIL FUNGUS SET

Manufacturer
Gaozhou Chapin Technology Co., Ltd
Effective date
2024-09-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:22:19

Label at a glance#

ProductFUHOP NAIL FUNGUS SET
Active ingredientTOLNAFTATE
Label structure12 sections

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Anti-fungal

Use

INDICATIONS & USAGE SECTION

Proven effective in the treatment of most athlete’s foot (tinea pedis)and ringworm(tinea corporis).

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 witheyes

Stop Use

OTC - STOP USE SECTION

If discomfort persists.

Ask Doctor

OTC - ASK DOCTOR SECTION

before you use 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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Melaleuca Alternifolia (Tea Tree)Leaf Oil , Water ,Glycerin , Allantoin,Allium Sativum (Garlic) Bulb Extract ，Cnidium Monnieri Fruit Extract ，Trimethoxysilylpropyl Steardimonium Chloride

DOSAGE & ADMINISTRATION SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabellabellabellabellabellabellabellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
313423tolnaftate 1 % Topical SolutionPSN1
313423tolnaftate 10 MG/ML Topical SolutionSCD1
313423tolnaftate 1 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84168-049-012025-07-29C16284748780-13b156c62-2a0a-fb37-e063-e6dba90a4e0723599feb-9588-3771-e063-6394a90af3eb

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84168-049-01FUHOP NAIL FUNGUS SET54 g in 1 BOXLIQUID541

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84168-049FUHOP NAIL FUNGUS SET (NAIL FUNGUS SET) LIQUID [GAOZHOU CHAPIN TECHNOLOGY CO., LTD]11 package rows20241001_23599feb-9588-3771-e063-6394a90af3eb.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
84168-04984168-049-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
GARLICV1V998DC17IACT
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OILVIF565UC2GIACT
WATER059QF0KO0RIACT
ALLANTOIN344S277G0ZIACT
GLYCERINPDC6A3C0OXIACT
CNIDIUM MONNIERI FRUITV1IA3S3CUSIACT
TOLNAFTATE06KB629TKVACTIB

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
2359c9ee-2605-3ee2-e063-6394a90a78aa23599feb-9588-3771-e063-6394a90af3eb2024-09-30WarningsExact identifier
spl id: 2359c9ee-2605-3ee2-e063-6394a90a78aa
spl set id: 23599feb-9588-3771-e063-6394a90af3eb

Reported adverse events (FAERS/openFDA)#

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