Active Ingredient(S)
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL、ALLANTOIN、TOCOPHEROL、ALOE VERA LEAF EXTRACT
Eelhoe Fungal Nail Treatment
FDA Label NDC 84660-037
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 Eelhoe Fungal Nail Treatment (NDC 84660-037). 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, warnings, use, storage and handling, do not use, stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Repair Nail
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.
Use
1.Clean and drythe affected toes and fingers thoroughly.
2.Gently file thick-ened part of the fungal nail with a nail file until it's flat or becomes thinner.
3.Apply a thin layer of liquid using the nail brush onto the affected area.
4.Repeat this process twice a day for 1-2 weeks or until the infection is gone.
Storage And Handling
Avoid freezing and excessive heat above 40C (104F) ）
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.
Inactive Ingredient
AQUA
Package Label.Principal Display Panel
Label (Zxzly226yx01 30ml)
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