Active Ingredients
Tolnaftate 1%
Fuhop Nail Fungus Set
FDA Label NDC 84168-049
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Gaozhou Chapin Technology Co., Ltd for the product Fuhop Nail Fungus Set (NDC 84168-049). 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 ingredients, purpose, use, warnings, do not use, when using, stop use, ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Anti-fungal
Use
Proven effective in the treatment of most athlete’s foot (tinea pedis)and ringworm(tinea corporis).
Warnings
For external use only
Do Not Use
■On irritated skin and any area that is infected or reddened.
■If pregnant or if there is any allergic reaction to this product.
When Using
avoid contact witheyes
Stop Use
If discomfort persists.
Ask Doctor
before you use If you have diabetes or poor blood circulation.
Keep Out Of Reach Of Children
■If product gets into eyes, flush with water for 15 minutes
■If swallowed, get medical help or contact a Poison Control Center right away.
Inactive Ingredients
Melaleuca Alternifolia (Tea Tree)Leaf Oil , Water ,Glycerin , Allantoin,Allium Sativum (Garlic) Bulb Extract ，Cnidium Monnieri Fruit Extract ，Trimethoxysilylpropyl Steardimonium Chloride
Dosage & Administration Section
One patch per day, each patch contains 1 mg of tolnaftate
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