Otc - Active Ingredient
Zingiber Officinale (Ginger) Root Extract
Sefudun Nail Fungus Treatment Liquid
FDA Label NDC 83804-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Shandian Jingling Technology Co., Ltd. for the product Sefudun Nail Fungus Treatment (NDC 83804-002). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
NAIL FUNGUS TREATMENT
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN SECTION
Indications & Usage
SEFUDUN 7-Day Nail Fungus Treatment is designed to repair and strengthen nails and cuticles, promoting healthier and stronger nails for both handsand feet.
Warnings
For external use only
Dosage & Administration
HOW TO USE:
1.Gently file the affected area to improveabsorption of the treatment.
2. Clean the surface with a dry swabor cloth.
3. Apply the formula evenly to theentire infected nail.
4. For optimal results, apply the treatmenttwice daily (morning & evening) for aminimum of 4 weeks
Inactive Ingredient
Aqua
Helianthus Annuus (Sunflower) Seed Oil
Hydrogenated Jojoba Oil
Package Label.Principal Display Panel
Label (Label)
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