Quick answers
- What is Econazole nitrate used for?
- The FDA-approved label (Ecoza, Resilia Pharmaceuticals, Inc., December 4, 2023) says: “Ecoza (econazole nitrate) topical foam, 1%, is indicated for the treatment of interdigital tinea pedis caused by Trichophyton rubrum, Trichophyton mentagrophytes, and Epidermophyton floccosum in patients 12 years of age and older. …” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
- Does Econazole nitrate have a boxed warning?
- No. None of the 13 FDA labels we found for this medicine has a boxed warning.
- Is there a shortage of Econazole nitrate?
- No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
- Has Econazole nitrate been recalled?
- No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
- Who makes Econazole nitrate?
- 8 companies list prescription products of Econazole nitrate in the FDA NDC Directory, including Bryant Ranch Prepack, Preferred Pharmaceuticals Inc. and Padagis Israel Pharmaceuticals Ltd.
What Econazole nitrate is used for
Quoted from the “Indications and Usage” section of the FDA-approved label.
Ecoza (econazole nitrate) topical foam, 1%, is indicated for the treatment of interdigital tinea pedis caused by Trichophyton rubrum, Trichophyton mentagrophytes, and Epidermophyton floccosum in patients 12 years of age and older. …
— FDA label: Ecoza, Resilia Pharmaceuticals, Inc., effective December 4, 2023. Read the full label on DailyMed →
The FDA has 13 labels for products of this medicine (different makers and forms); uses can differ between them. Check the label that comes with your own medicine.
This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Boxed warning
A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.
The label quoted above has no boxed warning.
0 of 13 FDA labels for this medicine have a boxed warning.
Forms and how it is given
| Dosage forms | Cream · Aerosol, foam |
|---|---|
| Route | Topical |
| Prescription products | 13 in the FDA NDC Directory |
| Brand names | Ecoza |
What pharmacies pay (NADAC)
The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.
This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.
| Strength and form | Generic or brand | Pharmacies pay |
|---|---|---|
| econazole nitrate 1% cream | Generic | $0.2086–$0.4028 per gram 6 packages, lowest to highest |
NADAC list of November 4, 2026; these prices took effect on October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.
Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →
Companies that list this medicine
Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.
- Bryant Ranch Prepack4 products
- Preferred Pharmaceuticals Inc.3 products
- Padagis Israel Pharmaceuticals Ltd1 product
- Aurobindo Pharma Limited1 product
- Resilia Pharmaceuticals, Inc.1 product
- Encube Ethicals, Inc.1 product
- Sun Pharmaceutical Industries, Inc.1 product
- Trifluent Pharma, LLC1 product
FDA approval history
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Sponsor | Approved | Later changes approved |
|---|---|---|---|
| NDA205175 ECOZA | Resilia Pharms | October 24, 2013 | 2, latest November 18, 2019 2019: Labeling · 2016: Manufacturing (CMC) |
Generic approvals (4)
- ANDA076005Sun Pharma Canada · November 26, 2002
- ANDA076479Padagis Israel · June 23, 2004
- ANDA076574Encube · December 17, 2004
- ANDA210364Aurobindo Pharma USA · April 18, 2018
Shortage status
The FDA drug shortage list does not show these products.
Recalls
No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.
Official identifiers
| RxCUI (RxNorm) | 857366, 1442585, 1442590 |
|---|---|
| SPL set ID of the quoted label | 0bb5fa27-32ed-ed13-e063-6394a90a1577 |
| FDA labels (SPL) | 13 |
| FDA applications | NDA205175, 4 ANDA |
| Active ingredients (FDA) | ECONAZOLE |
Sources
- FDA-approved label on DailyMed (National Library of Medicine) — Ecoza, Resilia Pharmaceuticals, Inc., effective December 4, 2023; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →