Inlifay ANTIFUNGAL
Inlifay ANTIFUNGAL is an FDA drug label for the active ingredient MICONAZOLE NITRATE 2% ANTIFUNGAL manufactured by Jiangxi Yudexi Pharmaceutical Co., LTD administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260906.
- Generic name
- MICONAZOLE NITRATE 2% ANTIFUNGAL
- Manufacturer
- Jiangxi Yudexi Pharmaceutical Co., LTD
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 85248-139
- Application
- M005
- Label effective
- 20260906
About this product
Inlifay ANTIFUNGAL is an FDA-registered drug product whose active ingredient is MICONAZOLE NITRATE 2% ANTIFUNGAL. It is labelled by Jiangxi Yudexi Pharmaceutical Co., LTD taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85248-139, application M005, label effective 20260906. 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.
What it is used for
Across FDA labelling, products containing MICONAZOLE NITRATE 2% ANTIFUNGAL are most often described in connection with: helps relieve, itching burning, scaling associated, fungal infections, athlete foot, jock itch. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use Helps relieve the itching, burning, cracking, and scaling associated with fungal infections such as athlete's foot,jock itch, and ringworm.
Dosage & Administration
Directions Clean the affected area and dry thoroughly. Apply a thin layer to the affected area twice daily (morning and night). Supervise children in the use of this product. Use daily for the full treatment period as directed. This product is not effective on the scalp or nails.
Warnings
Warnings For external use only.
More products with the same ingredient
MICONAZOLE NITRATE 2% ANTIFUNGALHow products containing MICONAZOLE NITRATE 2% ANTIFUNGAL compare
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.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | PureTek Corporation | 2 |
| — | — | Jiangxi Yudexi Pharmaceutical Co., LTD | 1 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is Inlifay ANTIFUNGAL used for?
Use Helps relieve the itching, burning, cracking, and scaling associated with fungal infections such as athlete's foot,jock itch, and ringworm.
Who makes Inlifay ANTIFUNGAL?
Jiangxi Yudexi Pharmaceutical Co., LTD is the labeler of record for Inlifay ANTIFUNGAL. 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 Inlifay ANTIFUNGAL 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 Inlifay ANTIFUNGAL 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 Inlifay ANTIFUNGAL 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.