Active Ingredient
TOLNAFTATE 1
Fungal Nail Patches
FDA Label NDC 84168-022
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 Fungal Nail Patches (NDC 84168-022). 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, 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
bacteriostatic, sterilizing
Use
Use for fungal nail infections
Warnings
For external use only
Do Not Use
It is prohibited for those who are allergic to this product and pregnant women, and should be used with caution on open wounds.
When Using
Do not put in eyes,If it accidentally gets into your eyes, rinse with water or seek medical advice.If irritation or rash occurs, discontinue use and ask a doctor. If swallowed, get medical help or contact a Poison Control Center immediately
Stop Use
Stop use and ask a doctor if irritation or rash occurs
Ask Doctor
Do not put in eyes,lfit accidentally gets into your eyes, rinse with water or seek medical advice.lfirritation or rash occurs, discontinue use and ask a doctor. if swallowed, get medical help orcontact a Poison Control Centerimmediate.
Keep Oot Of Reach Of Children
Please keep this product out of reach of children
Dosage & Administration Section
One patch per day, each patch contains 1 mg of tolnaftate
Inactive Ingredients
Glycerin, Allantoin,Allium Sativum (Garlic) Bulb Extract,Cnidium,Monnieri Fruit Oil,Melaleuca Alternifolia (Tea Tree) Leaf oil
Package Label.Principal Display Panel
Label (20405)
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