AlJIEYO Fungal Nail Treatment Liquid

Manufacturer
Shenzhen Yikai Electronic Technology Co., Ltd.
Effective date
2023-12-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:05:47

Label at a glance#

ProductAlJIEYO Fungal Nail Treatment Liquid
Active ingredientUNDECYLENIC ACID
Label structure9 sections

Dosage and administration

shake well before use. Wash and thoroughly dry the affected area. Apply 1-2 drops and gently rub into affected area three times per day. Wash hands after applying.

Storage and handling

*Keep in cool dark place *Store upright *Tighten cap after use to prevent oxidation

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Undecylenic acid 10%

Purpose

OTC - PURPOSE SECTION

Anti-fungal

Use

INDICATIONS & USAGE SECTION

for relief and treatment of pain,
soreness, and inflammation from nail
fungus. Symptoms:

■discolored nails
■brittle nails

■distorted nails

Warnings

WARNINGS SECTION

For external use only. Some individuals may be sensitive to essential oils. Begin with a small drop to determine if product causes any irritation. Discontinue use if any irritation occurs. Stop use and consult a doctor if condition worsens. Not for use on children under the age of 2 without physician direction.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If pregnant or breast-feeding, ask a health professional before use. If accidental ingestion and adverse reaction occurs, get medical help or contact a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

shake well before use. Wash and thoroughly dry the affected area. Apply 1-2 drops and gently rub into affected area three times per day. Wash hands after applying.

Other information

STORAGE AND HANDLING SECTION

*Keep in cool dark place
*Store upright
*Tighten cap after use to prevent
oxidation

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,Lonicerae Japonicae flos,Angelicae,Glycerin, Allantoin, Garlic Extract, Tea Tree Oil.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

001001002002

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1251008undecylenic acid 10 % Topical SolutionPSN1
1251008undecylenic acid 100 MG/ML Topical SolutionSCD1
1251008undecylenic acid 10 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83809-015-012025-01-30C16284748780-12cef2736-a15b-d83d-e063-dadaa90ab31f83809-015

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83809-015-01AlJIEYO Fungal Nail Treatment Liquid20 mL in 1 BOTTLELIQUID201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83809-015ALJIEYO FUNGAL NAIL TREATMENT LIQUID LIQUID [SHENZHEN YIKAI ELECTRONIC TECHNOLOGY CO., LTD.]11 package rows20231228_0d78aae8-38f6-432c-e063-6394a90a461b.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
83809-01583809-015-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
0d78aae8-38f7-432c-e063-6394a90a461b0d78aae8-38f6-432c-e063-6394a90a461b2023-12-27WarningsExact identifier
spl id: 0d78aae8-38f7-432c-e063-6394a90a461b
spl set id: 0d78aae8-38f6-432c-e063-6394a90a461b

Reported adverse events (FAERS/openFDA)#

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