Otc - Active Ingredient
Glycerin 1%
Sefudun Fungal Nail Patches Patch
FDA Label NDC 83804-006
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 Fungal Nail Patches (NDC 83804-006). 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, indications & usage, warnings, otc - do not use, otc - when using, otc - 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
Otc - Purpose
antifungal
Indications & Usage
REDUCES DISCOLOR-ATION & THICKNESS, REVITALIZESBRITTLE NAILS，IMPROVES NAILAPPEARANCE
Warnings
For extemal use only.
Otc - Do Not Use
Not recommended whilepregnant or breastfeeding.
Otc - When Using
Avoid contact with eyes, mouth, mucous membranes and wounds.
Otc - Stop Use
Discontinue use if an allergic reaction occurs.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN SECTION
Dosage & Administration
Clean and dry the affecled area before application. Remove the prolective filmand peel off the release paper from the patch. Place the sticky side of the patchdirectiy onto the infected area of the nail. Gently fold the sides of the paich arotndyour toe or finger for secure adherence. Leave the patch on for 6.8 hours, ideallyovernight, to allow for effective treatment.
Inactive Ingredient
Polyester, Silicone Oil
Package Label.Principal Display Panel
Label1 (Label1)
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