SSPROTIP X Extra Strength Nail Renewal Patches

SSPROTIP X Extra Strength Nail Renewal Patches is an FDA-registered drug product whose active ingredient is TOLNAFTATE. It is labelled by GUANGZHOU SAWEILAN IMPORT & EXPORT TRADING CO., LTD taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85966-016, application M005, label effective 20260521. 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: athlete foot, tinea pedis, jock itch, effective treatment, relief itching, scaling cracking, burning redness, soreness irritation. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

For effective treatment of most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis). For effective relief of itching, scaling, cracking, burning, redness, soreness, irritation, discomfort and chafing associated with jock itch. Proven effective in the prevention of most athlete's foot (tinea pedis) with daily use.

Clean and dry the affected nail. For best results, gently file down thickened areas before application. Peel off the protective film. Align the active gel center directly over the nail, ensuring full coverage of the surface and edges. Press the pear-shaped base to the nail root, wrap the tapered top over the fingertip, and hold firmly for 10s. Keep the patch on for 24 hours. Replace it once a day (increase frequency for severe cases). Clean the nail thoroughly between replacing. The patch is water-resistant for showers. Avoid soaking for over 30 minutes. Use a waterproof cover if swimming or bathing. Use consistently until the damaged nail is fully replaced by healthy, clear growth. Full restoration may take several months. This product is not effective on the scalp or nails.

For external use only. Store in a cool place and avoid sunshine and heat.

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 SSPROTIP X Extra Strength Nail Renewal Patches used for?
For effective treatment of most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis). For effective relief of itching, scaling, cracking, burning, redness, soreness, irritation, discomfort and chafing associated with jock itch. Proven effective in the prevention of most athlete's foot (tinea pedis) with daily use.

Who makes SSPROTIP X Extra Strength Nail Renewal Patches?
GUANGZHOU SAWEILAN IMPORT & EXPORT TRADING CO., LTD is the labeler of record for SSPROTIP X Extra Strength Nail Renewal Patches. 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 SSPROTIP X Extra Strength Nail Renewal Patches 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 SSPROTIP X Extra Strength Nail Renewal Patches 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 SSPROTIP X Extra Strength Nail Renewal Patches 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.