EZBIORT 1% Tolnaftate Nail Essence with Biotin

EZBIORT 1% Tolnaftate Nail Essence with Biotin is an FDA-registered drug product whose active ingredient is TOLNAFTATE. It is labelled by Guangzhou Borderless Technology Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85304-032, application M005, label effective 20260709. It is one of 53 FDA drug label records sharing the active ingredient TOLNAFTATE. 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 are most often described in connection with: antifungal treatment, fingernails toenails, surrounding skin, effective against, fungal nails, athlete foot, caused fungi. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Antifungal treatment for fingernails,toenails, and surrounding skin.Effective against fungal nails and athlete's foot caused by fungi

For athlete's foot and ringworm: use daily for 4 weeks.Clean the affected area and dry thoroughly. For external use on nails and the immediately adjacent skin only. Twice a day lonce in the morning and once in the evening), apply or spray the medicine on the nails. Afterwards, the medicine will be able to penetrate deeply into the interior of the nails. If the nail area is infected, spray the medication onto the affected area. SHAKE WELL BEFORE USE. Store at 5°C to 30°C(41°F to 86F) in a cool dry place. Keep tightly closed and away from sunlight.

For external use only.

FDA lists 53 drug label records with TOLNAFTATE 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 EZBIORT 1% Tolnaftate Nail Essence with Biotin used for?
Antifungal treatment for fingernails,toenails, and surrounding skin.Effective against fungal nails and athlete's foot caused by fungi

Who makes EZBIORT 1% Tolnaftate Nail Essence with Biotin?
Guangzhou Borderless Technology Co., Ltd. is the labeler of record for EZBIORT 1% Tolnaftate Nail Essence with Biotin. 53 FDA label records share the active ingredient TOLNAFTATE, 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 EZBIORT 1% Tolnaftate Nail Essence with Biotin 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 EZBIORT 1% Tolnaftate Nail Essence with Biotin 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?
Yes. 53 FDA drug label records list TOLNAFTATE 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 EZBIORT 1% Tolnaftate Nail Essence with Biotin 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.