Lasolex AC

Lasolex AC is an FDA-registered drug product whose active ingredient is MICONAZOLE NITRATE 2% ANTIFUNGAL. It is labelled by PureTek Corporation taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 59088-239, application M005, label effective 20260603. It is one of 3 FDA drug label records sharing the active ingredient MICONAZOLE NITRATE 2% ANTIFUNGAL. 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 2% ANTIFUNGAL are most often described in connection with: jock itch, athlete foot, tinea pedis, relief itching, scaling cracking, burning redness, soreness irritation, discomfort chafing. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For the treatment of most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis). For relief of itching, scaling, cracking, burning, redness, soreness, irritation, discomfort, chafing associated with jock itch, itchy, scaly skin between the toes, or itching, burning feet.

Directions Wash the affected area and dry thoroughly. Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor • Supervise children in the use of this product. For athlete's foot: Pay special attention to the spaces between the toes; Wear well fitting, ventilated shoes, and change shoes and socks atleast 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 nails.

Warnings For external use only.

FDA lists 3 drug label records with MICONAZOLE NITRATE 2% ANTIFUNGAL 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 Lasolex AC used for?
Uses For the treatment of most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis). For relief of itching, scaling, cracking, burning, redness, soreness, irritation, discomfort, chafing associated with jock itch, itchy, scaly skin between the toes, or itching, burning feet.

Who makes Lasolex AC?
PureTek Corporation is the labeler of record for Lasolex AC. 3 FDA label records share the active ingredient MICONAZOLE NITRATE 2% ANTIFUNGAL, 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 Lasolex AC 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 Lasolex AC 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 2% ANTIFUNGAL?
Yes. 3 FDA drug label records list MICONAZOLE NITRATE 2% ANTIFUNGAL 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 Lasolex AC 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.