FDA.reportPublic FDA data

7 Days Nail Fungus Treatment

Manufacturer
Guangdong Ximonth Technology Co., Ltd.
Effective date
2024-08-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:18:09

Label at a glance#

Product7 Days Nail Fungus Treatment
Active ingredientSUNFLOWER OIL, SODIUM SULFIDE, HYDROGENATED JOJOBA OIL
Label structure9 sections

Storage and handling

Avoid freezing and excessive heat above 40C (104F) ） Store in a cool and dry place.

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Restores damage nail & cuticle

Use

OTC - WHEN USING SECTION

1.File the area affected by the nail to enhance the permeability of the essence.2.Clean the surface with a dry swab /cloth.3.Apply the essence to the entire surface of the infected nail.4.Apply the cream twice a day (morning and evening) for at least 4 weeks.

Warnings

WARNINGS SECTION

Please keep out of reach of children.Do not swallow.Please clean your hands before use to ensure the best results from the product.Discontinue use if signs of irritation or rash occur.Store in a cool and dry place.

Do not use

OTC - DO NOT USE SECTION

Discontinue use if signs of irritation or rash occur.

STOP USE

OTC - STOP USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep out of reach of children. Do not swallow.

STORAGE AND HANDLING SECTION

Avoid freezing and excessive heat above 40C (104F) ）

Store in a cool and dry place.

INACTIVE INGREDIENT SECTION

AQUA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84660-004-017 Days Nail Fungus Treatment30 mg in 1 BOXLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84660-0047 DAYS NAIL FUNGUS TREATMENT (SODIUM SULFIDE) LIQUID [GUANGDONG XIMONTH TECHNOLOGY CO., LTD.]11 package rows20240830_20bc7db1-ae1e-862b-e063-6394a90a5fd1.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84660-00484660-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUNFLOWER OIL3W1JG795YIACTIB
ALLANTOIN344S277G0ZIACT
SODIUM SULFIDEYGR27ZW0Y7ACTIB
HYDROGENATED JOJOBA OIL7F674YQ5SOACTIB
WATER059QF0KO0RIACT

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
20bc7db1-ae1f-862b-e063-6394a90a5fd120bc7db1-ae1e-862b-e063-6394a90a5fd12024-08-28WarningsExact identifier
spl id: 20bc7db1-ae1f-862b-e063-6394a90a5fd1
spl set id: 20bc7db1-ae1e-862b-e063-6394a90a5fd1

Reported adverse events (FAERS/openFDA)#

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