Osimoon Fungal Nail Treatment Kit

Manufacturer
Guangzhou Zanming Trading Co., Ltd.
Effective date
2025-05-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:00:42

Label at a glance#

ProductOsimoon Fungal Nail Treatment Kit
Active ingredientUNDECYLENIC ACID
Label structure13 sections

Dosage and administration

• Clean the affected area with soap, soak the nail in warm water to soften it. • Then let it dry, apply a thin layer of the antifungal solution included in the kit 2-3 times a day. • Apply the fungus nail patch once a night. Firmly secure the patch to the sides of the toes or fingers, folding the remaining adhesive part to fully cover the toes/fingertips. • Keep the patch in this position for 6-8 hours, preferably...

Storage and handling

Store at room temperature. Reseal pouch after each use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Undecylenic Acid 10% W/W

Purpose

OTC - PURPOSE SECTION

Antifungal

Use

INDICATIONS & USAGE SECTION

Effective in getting rid of fungus and promoting healthier nail growth.

Warnings

WARNINGS SECTION

• For external use only.
• When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.
• Stop use and ask/ consult a doctor/ physician/ health care practitioner/ health care provider/ health care professional if irritation or symptoms worsen or last for more than 4 weeks.
• Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away.

Do not use

OTC - DO NOT USE SECTION

• If you are pregnant or breastfeeding
• your skin is injured or cracked.
• you are under 18 years of age.
• irritation or discomfort occurs.
• you are using other medicines on your nails.

When Using

OTC - WHEN USING SECTION

• Do not apply to other parts of the body.
• Avoid making eye contact. In case of accidental eye contact, flush eyes with copious amounts of cold tap water.
• This product may not work for everyone.

Stop Use

OTC - STOP USE SECTION

if irritation or symptoms worsen or last for more than 4 weeks.

Ask Doctor

OTC - ASK DOCTOR SECTION

if irritation or symptoms worsen or last for more than 4 weeks.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Clean the affected area with soap, soak the nail in warm water to soften it.
• Then let it dry, apply a thin layer of the antifungal solution included in the kit 2-3 times a day.
• Apply the fungus nail patch once a night. Firmly secure the patch to the sides of the toes or fingers, folding the remaining adhesive part to fully cover the toes/fingertips.
• Keep the patch in this position for 6-8 hours, preferably overnight, and recommended for 3-6 months.

Other information

STORAGE AND HANDLING SECTION

Store at room temperature. Reseal pouch after each use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Mineral oil, Apricot Kernel Oil, Tea Tree Oil,Tocopherol, Peppermint Oil, Camphor Oil, Jojoba Oil, Bergamot Oil, Lavender Oil, Hydrogel, Elastic fabric, Adhesive, Release paper

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
2db4fc38-a116-b0ab-3dae-57df54e5f212Product name220250121
386d1b2a-e9b7-0c83-111f-2a77b92895b3Product name520240422
7d55b53c-798b-47ae-992b-3921493a8303Product name120230322
8d753fd6-75b2-4f12-bcbf-339392960afaProduct name120230303
4fbda828-a5be-46fe-83ec-a88da4359919Product name120230104
93cc9bee-8bdc-273d-ec7f-c2c52535317aProduct name720210902
a6389cd1-36d1-4b5c-9934-1139bee93605Product name520210601
f4f0889f-ee8b-471f-9a37-02a035280637Product name120200122
09e1afd3-f431-4380-82c5-438884c25615Product name120190111
a6389cd1-36d1-4b5c-9934-1139bee93605Product name320171212
502efed8-01a5-ef6a-61c6-fe8302b6e26bProduct name220171113
8b700cfd-17dd-41a2-90f5-a80ae8a989a2Product name120171113
9ce0e503-4ae7-2c6a-39ae-85285c29db68Product name220171113
96bdf4b3-71cd-433d-9723-89e50f852992Product name120150810
ed2e617f-f28a-1df1-f9fc-c79702f31271Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85150-008-01Osimoon Fungal Nail Treatment Kit15 mL in 1 BOTTLELIQUID151
85150-008-01Osimoon Fungal Nail Treatment Kit2 in 1 BOXLIQUID21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85150-008OSIMOON FUNGAL NAIL TREATMENT KIT LIQUID [GUANGZHOU ZANMING TRADING CO., LTD.]1Current NDC, 2 package rows20250510_34aec10d-a0d0-d956-e063-6394a90a39b2.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85150-00885150-008-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
Osimoon Fungal Nail Treatment KitOSIMOON FUNGAL NAIL TREATMENT KITGuangzhou Zanming Trading Co., Ltd.34aec10d-a0d0-d956-e063-6394a90a39b22025-05-09WarningsExact identifier
ndc (package): 85150-008-01
ndc (product): 85150-008
ndc11 (package): 85150000801
spl id: 34aec10d-a0d1-d956-e063-6394a90a39b2
spl set id: 34aec10d-a0d0-d956-e063-6394a90a39b2

Reported adverse events (FAERS/openFDA)#

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