Antifungal Powder

Antifungal Powder is an FDA-registered drug product whose active ingredient is MICONAZOLE NITRATE. It is labelled by Aldermed Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87236-012, application M005, label effective 20260608. It is one of 70 FDA drug label records sharing the active ingredient MICONAZOLE NITRATE. 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 MICONAZOLE NITRATE are most often described in connection with: jock itch, proven clinically, athlete foot, ringworm relieves, itching scaling, cracking burning, redness soreness, discomforts associated. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses • Proven clinically effective in the treatment of most: • athlete's foot • jock itch • ringworm • Relieves itching, scaling, cracking, burning, redness, soreness, irrita-tion, and discomforts associated with all three treatments. Also relieves chaffing associated with jock itch.

Directions ■ clean affected area and dry thoroughly ■ apply thin layer of powder to affected area twice daily (morning and night) or as direct-ed by a doctor ■ supervise children in the use of this product ■ for athlete's foot pay special attention to space between the toes; wear well-fitting, ventilated shoes and change shoes and socks at least once daily • for athlete's foot and ringworm, use daily for 4 weeks; for jock itch use daily for 2 weeks ■ if condition persists longer, consult a doctor •this product is not effective on the scalp or nail

Warnings For external use only.

FDA lists 70 drug label records with MICONAZOLE NITRATE 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.

1 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

What is Antifungal Powder used for?
Uses • Proven clinically effective in the treatment of most: • athlete's foot • jock itch • ringworm • Relieves itching, scaling, cracking, burning, redness, soreness, irrita-tion, and discomforts associated with all three treatments. Also relieves chaffing associated with jock itch.

Who makes Antifungal Powder?
Aldermed Inc. is the labeler of record for Antifungal Powder. 70 FDA label records share the active ingredient MICONAZOLE NITRATE, 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 Antifungal Powder 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 Antifungal Powder 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 MICONAZOLE NITRATE?
Yes. 70 FDA drug label records list MICONAZOLE NITRATE 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 Antifungal Powder been recalled?
1 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

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.