FUHOP Fungal Nail Liquid

Manufacturer: Gaozhou Chapin Technology Co., Ltd
Effective date: 2024-09-05
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:18:53

Label at a glance#

ProductFUHOP Fungal Nail Liquid

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

Water,Glycerin, Allantoin, Alum Sativum (Garlic) Bulb Extact, Melaleuca Alternifolia (Tea Tree) Leaf Oil

DOSAGE & ADMINISTRATION SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
313423	tolnaftate 1 % Topical Solution	PSN	1
313423	tolnaftate 10 MG/ML Topical Solution	SCD	1
313423	tolnaftate 1 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
84168-042-02	2025-07-29	C162847	48780-1	3b156c62-2757-fb37-e063-e6dba90a4e07	215e0fc4-c06b-08e1-e063-6294a90aa9fc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84168-042-02	FUHOP Fungal Nail Liquid	10 mL in 1 BOTTLE, PUMP	LIQUID	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84168-042	FUHOP FUNGAL NAIL LIQUID (FUNGAL NAIL LIQUID) LIQUID [GAOZHOU CHAPIN TECHNOLOGY CO., LTD]	1	1 package rows	20240906_215e0fc4-c06b-08e1-e063-6294a90aa9fc.zip

Products#

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

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

FUHOP Fungal Nail Liquid
Fungal Nail Liquid
GARLIC
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL
WATER
ALLANTOIN
GLYCERIN
TOLNAFTATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84168-042	84168-042-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GARLIC	V1V998DC17	IACT
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL	VIF565UC2G	IACT
WATER	059QF0KO0R	IACT
ALLANTOIN	344S277G0Z	IACT
GLYCERIN	PDC6A3C0OX	IACT
TOLNAFTATE	06KB629TKV	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
215e0fcc-a551-3660-e063-6294a90a35ea			215e0fc4-c06b-08e1-e063-6294a90aa9fc	2024-09-05	Warnings	Exact identifier spl id: 215e0fcc-a551-3660-e063-6294a90a35ea spl set id: 215e0fc4-c06b-08e1-e063-6294a90aa9fc

Reported adverse events (FAERS/openFDA)#

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