PUVIDA FUNGAL NAIL

PUVIDA FUNGAL NAIL is an FDA-registered drug product whose active ingredient is TOLNAFTATE 1% FUNGAL NAIL. It is labelled by Jiangxi Yudexi Pharmaceutical Co., LTD taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85248-153, application M005, label effective 20260614. It is one of 3 FDA drug label records sharing the active ingredient TOLNAFTATE 1% FUNGAL NAIL. 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.

Across FDA labelling, products containing TOLNAFTATE 1% FUNGAL NAIL 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.

Use Repairs fungal nail damage and improves nail appearance

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 For external use only.

FDA lists 3 drug label records with TOLNAFTATE 1% FUNGAL NAIL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is PUVIDA FUNGAL NAIL used for?
Use Repairs fungal nail damage and improves nail appearance

Who makes PUVIDA FUNGAL NAIL?
Jiangxi Yudexi Pharmaceutical Co., LTD is the labeler of record for PUVIDA FUNGAL NAIL. 3 FDA label records share the active ingredient TOLNAFTATE 1% FUNGAL NAIL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does PUVIDA FUNGAL NAIL 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 PUVIDA FUNGAL NAIL 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.

Are there other products containing TOLNAFTATE 1% FUNGAL NAIL?
Yes. 3 FDA drug label records list TOLNAFTATE 1% FUNGAL NAIL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has PUVIDA FUNGAL NAIL 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.