Active Ingredient(S)
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL,HYDROGENATED JOJOBA OIL,ALLANTOIN,SODIUM SULFIDE
7 Days Nail Fungus Treatment
FDA Label NDC 84660-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Ximonth Technology Co., Ltd. for the product 7 Days Nail Fungus Treatment (NDC 84660-010). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient(s), purpose, use, warnings, do not use, stop use, otc - keep out of reach of children, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Restores damage nail & cuticle
Use
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
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
Discontinue use if signs of irritation or rash occur.
Stop Use
Discontinue use if signs of irritation or rash occur.
Otc - Keep Out Of Reach Of Children
Please keep out of reach of children. Do not swallow.
Storage And Handling
Avoid freezing and excessive heat above 40C (104F) ）
Store in a cool and dry place.
Inactive Ingredient
AQUA
Package Label.Principal Display Panel
Label (Jzjxhy809cy01 30ml)
* Please review the disclaimer below.
