HuiPoLii NAIL PFLASTER
HuiPoLii NAIL PFLASTER is an FDA drug label for the active ingredient TOLNAFTATE 1% NAIL PFLASTER manufactured by Jiangxi Yudexi Pharmaceutical Co., LTD administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260508.
- Generic name
- TOLNAFTATE 1% NAIL PFLASTER
- Manufacturer
- Jiangxi Yudexi Pharmaceutical Co., LTD
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 85248-206
- Application
- M005
- Label effective
- 20260508
About this product
HuiPoLii NAIL PFLASTER is an FDA-registered drug product whose active ingredient is TOLNAFTATE 1% NAIL PFLASTER. It is labelled by Jiangxi Yudexi Pharmaceutical Co., LTD taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85248-206, application M005, label effective 20260508. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing TOLNAFTATE 1% NAIL PFLASTER are most often described in connection with: repairs fungal, nail damage. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use Repairs fungal nail damage and improves nail appearance
Dosage & Administration
Directions Clean and thoroughly dry the affected area before application. ■Peel off the patch's protective film, starting with the outer side and then the inner side. ■Place the sticky side of the patch directly onto the infected area on the nail and remove the release paper. Gently wrap the sides of the toe or finger to ensure a snug fit. ■Fold the remaining adhesive part to cover the toe/fingertip. Leave the patch onfor 6-8 hours (It is recommended to use overnight for 3-6 months).
Warnings
Warnings For external use only.
Frequently asked questions
What is HuiPoLii NAIL PFLASTER used for?
Use Repairs fungal nail damage and improves nail appearance
Who makes HuiPoLii NAIL PFLASTER?
Jiangxi Yudexi Pharmaceutical Co., LTD is the labeler of record for HuiPoLii NAIL PFLASTER.
What form does HuiPoLii NAIL PFLASTER come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is HuiPoLii NAIL PFLASTER prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has HuiPoLii NAIL PFLASTER been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.