Kopa Haiku Antifungal Cream
Kopa Haiku Antifungal Cream is an FDA drug label for the active ingredient MICONAZOLE NITRATE 2% manufactured by Trovina 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 20260602.
- Generic name
- MICONAZOLE NITRATE 2%
- Manufacturer
- Trovina Co. Ltd
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87041-002
- Application
- M005
- Label effective
- 20260602
About this product
Kopa Haiku Antifungal Cream is an FDA-registered drug product whose active ingredient is MICONAZOLE NITRATE 2%. It is labelled by Trovina Co. Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87041-002, application M005, label effective 20260602. It is one of 24 FDA drug label records sharing the active ingredient MICONAZOLE NITRATE 2%. 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% are most often described in connection with: effective treatment, 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
Anti-fungal for the effective treatment of Athlete's Foot, Jock Itch, Ringworm.
Dosage & Administration
1 Apply a small amount of cream to the affected area 2-3 times daily; 2 Ensure the skin in clean and dry before use; 3 For first-time users, perform a patch test on a small area of skin to check for sensitivity.
Warnings
For external use only On children under 3 years of age. Avoid contact with the eyes. Irritation occurs or if there is no improvement within 4 weeks. Keep out of reach of children. In case of ingestion, seek medical help or contact a Poison Control Center immediately.
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View labelHow products containing MICONAZOLE NITRATE 2% compare
FDA lists 24 drug label records with MICONAZOLE NITRATE 2% 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 |
|---|---|---|---|
| — | — | Jiangxi Yudexi Pharmaceutical Co., LTD | 5 |
| — | — | Trovina Co. Ltd | 4 |
| — | — | Wenzhou Yuyuan Pharmaceutical Co., Ltd. | 4 |
| — | — | PureTek Corporation | 2 |
| — | — | REGENEREN PLUS LTD | 2 |
Frequently asked questions
What is Kopa Haiku Antifungal Cream used for?
Anti-fungal for the effective treatment of Athlete's Foot, Jock Itch, Ringworm.
Who makes Kopa Haiku Antifungal Cream?
Trovina Co. Ltd is the labeler of record for Kopa Haiku Antifungal Cream. 24 FDA label records share the active ingredient MICONAZOLE NITRATE 2%, 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 Kopa Haiku Antifungal Cream 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 Kopa Haiku Antifungal Cream 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%?
Yes. 24 FDA drug label records list MICONAZOLE NITRATE 2% 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 Kopa Haiku Antifungal Cream 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.