KDMAN

KDMAN is an FDA-registered drug product whose active ingredient is TOLNAFTATE. It is labelled by Dongguan Youmi Trading Co., Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87723-6625, application M005, label effective 20260525. 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: cures athlete, foot tinea, pedis jock, corporis relieves, itching burning, conditions provides, fast relief, skin irritation. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Cures athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis). Relieves itching, burning, cracking and discomfort which accompany these conditions. Provides fast relief of skin irritation and odor.

Directions Use twice daily (morning and night) during a shower or bath, or as directed by a doctor. Apply the soap to the body and feet, gently massaging over the entire skin. Pay special attention to spaces between the toes and areas prone to odor or skin irritation. For best results, allow the lather to remain on the skin for 1 to 2 minutes before rinsing. Rinse and dry the skin and feet thoroughly. Supervise children in the use of this product. For athlete's foot and ringworm: use daily for 4 weeks. For jock itch: use daily for 2 weeks. This product is not effective on the scalp or nails.

Warnings For external use only. Do not use On children under 2 years of age unless directed by a doctor. When using this product Avoid contact with eyes. Stop use and ask a doctor if Irritation occurs. There is no improvement within 4 weeks for athlete's foot or ringworm, or 2 weeks for jock itch.

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 KDMAN used for?
Uses Cures athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis). Relieves itching, burning, cracking and discomfort which accompany these conditions. Provides fast relief of skin irritation and odor.

Who makes KDMAN?
Dongguan Youmi Trading Co., Ltd is the labeler of record for KDMAN. 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 KDMAN 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 KDMAN 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 KDMAN 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.