Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Miconazole Nitrate Antifungal Miconazole Powder Spray 2.6 g/130g Aerosol, Spray, 130 g — NDC 67091-392-06 (Billing 67091-0392-06)
by Winco Foods, LLC · 130 g in 1 CANISTER
This is a package of 130 g of Miconazole Nitrate Antifungal Miconazole Powder Spray 2.6 g/130g Aerosol, Spray from Winco Foods, LLC, marketed since Sep 2021 and currently FDA-listed. It is this product's only package size.
NDC 67091-0392-06
🏷️ FDA NDC (as labeled)
67091-392-06
billing pads the product segment with a zero
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
67091-392-06
Product NDC
67091-392
11-digit billing NDC
67091039206
RxCUI
998428
UNII
VW4H1CYW1K
Application #
M005
SPL Set ID
cc24f4ca-a403-0dc4-e053-2a95a90a5dad
Established class (EPC)
Azole Antifungal
Chemical class
Azoles
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2021-09-29
Route
TOPICAL
Dosage form
AEROSOL, SPRAY
Substance
MICONAZOLE NITRATE
Quick answers
- RxCUI (RxNorm): 998428
Why two NDCs?
The FDA registers this code as 67091-392-06 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 67091-0392-06. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
RxNorm drug class
This medicine belongs to the Azole Antifungal class.
Pharmacologic class
Azole Antifungal
Drug family (ATC)
Antiinfectives and antiseptics for local oral treatment, Imidazole derivatives, Imidazole and triazole derivatives
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
📖 What it is MedlinePlus · NLM
Topical miconazole is used to treat tinea corporis(ringworm; fungal skin infection that causes a red scaly rash on different parts of the body), tinea cruris (jock itch; fungal infection of the skin in the groin or buttocks), and tinea pedis (athlete's foot; fungal infection of the skin on the feet and between the toes). Miconazole is in a class of antifungal medications called imidazoles. It works by stopping the growth of fungi that cause infection. Not all products should be used to treat all of these conditions. Please read the label for each product to select the one to treat your conditi...
Read the full MedlinePlus article ↗📗 Our plain-language guide HelloPharmacist
- It treats fungal and yeast infections. Depending on the product, that means vaginal yeast infections, athlete's foot, jock itch, ringworm, or thrush in the mouth and throat (Oravig...
- Apply it to your upper gum in the morning after brushing, with dry hands. Hold it in place for 30 seconds. Don't crush, chew or swallow it. Use it once a day for 14 days.
- Most are mild, like diarrhea, nausea, headache, upper belly pain or a change in taste. Vaginal products may cause mild burning or itching at first. Stop and get help for hives, tro...
- Tell me if you take warfarin. Miconazole can boost its blood-thinning effect, so watch for bleeding or bruising. With Oravig, oral diabetes medicines, phenytoin and ergot alkaloids...
Patient education
Supplement & herbal interactions
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about Antifungal Miconazole Powder Spray?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per mL | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 2, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 67091-0392-06 You're viewing this Main listing | 130 g in 1 CANISTER | 2021-09-29 | — | Active |
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Miconazole Nitrate 2.6 g/130g 70000-0321-01 | Cardinal | 130 g | $0.036 | — | Availability likely | — |
| Miconazole Nitrate 2.6 g/130g 00363-7418-00 | Walgreens | 130 g | — | — | FDA listed | — |
| Lotrimin AF Jock Itch 20 mg/g 11523-0133-01 | Bayer | 133 g | — | — | FDA listed | — |
| Lotrimin AF 20 mg/g 11523-0134-01 | Bayer | 133 g | — | — | FDA listed | — |
| Lotrimin AF Deodorant 20 mg/g 11523-0135-01 | Bayer | 133 g | — | — | FDA listed | — |
| Miconazole Nitrate 2.6 g/130g 11822-0135-04 | Rite | 130 g | — | — | FDA listed | — |
| Miconazole Nitrate 2.6 g/130g 21130-0212-00 | Better | 130 g | — | — | FDA listed | — |
| Good Neighbor Pharmacy Jock Itch Relief Antifungal 20 mg/g 23667-0819-01 | Formulated | 130 g | — | — | Discontinued | — |
| Miconazole Nitrate 2.6 g/130g 36800-0384-46 | Topco | 130 g | — | — | FDA listed | — |
| Miconazole Nitrate 2.6 g/130g 41250-0196-46 | Meijer | 130 g | — | — | Discontinued | — |
| Miconazole Nitrate 2.6 g/130g 41520-0565-46 | Foodhold | 130 g | — | — | FDA listed | — |
| Silka Athletes Foot 20 mg/g 50066-0084-46 | Genomma | 130 g | — | — | FDA listed | — |
| Miconazole Nitrate 2.6 g/130g 56104-0121-01 | Premier | 130 g | — | — | FDA listed | — |
| Miconazole Nitrate 2.6 g/130g 56104-0131-46 | Premier | 130 g | — | — | Discontinued | — |
| Miconazole Nitrate 20 mg/g 56104-0907-01 | Premier | 130 g | — | — | FDA listed | — |
| Athletes Foot 20 mg/g 56104-0912-01 | Premier | 130 g | — | — | FDA listed | — |
| HEB Athlete Foot Antifungal 20 mg/g 59640-0101-01 | HEB | 130 g | — | — | FDA listed | — |
| Miconazole Nitrate 2.6 g/130g 63868-0180-46 | Chain | 130 g | — | — | FDA listed | — |
| Miconazole Nitrate 2.6 g/130gthis 67091-0392-06 | Winco | 130 g | — | — | FDA listed | — |
| Miconazole Nitrate 2.6 g/130g 69256-0039-46 | Harris | 130 g | — | — | FDA listed | — |
| Miconazole Nitrate 2.6 g/130g 69842-0511-46 | CVS | 130 g | — | — | FDA listed | — |
| Antifungal Athletes Foot 20 mg/g 79481-0505-01 | Meijer | 130 g | — | — | FDA listed | — |
| Jock Itch 20 mg/g 79481-0602-01 | Meijer | 130 g | — | — | FDA listed | — |
| Miconazole Nitrate 2.6 g/130g 79903-0014-46 | Wal-Mart | 130 g | — | — | FDA listed | — |
| Miconazole Nitrate 20 mg/g 83324-0233-46 | Chain | 130 g | — | — | FDA listed | — |
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2021
On the market since
Sep 2021
📍
2026
Currently FDA-listed
5 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.
- FDA Orange Book · refreshed Sep 3, 2026
Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII 3K9958V90M
A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
-
UNII X687XDK09L
A clay mineral processed to carry positive charges, used as a thickener and suspending agent in liquid medicines. It helps keep solid particles evenly distributed throughout the product.
-
UNII BXR49TP611
Isobutane is a liquefied gas used as a propellant in aerosol inhalers and sprays. It helps push the medicine out of the container so you can breathe or spray it as directed.
-
UNII 24H4NWX5CO
Kaolin is a naturally occurring clay mineral. It's used in tablets and capsules as a filler and absorbent to add bulk, improve texture, and help bind ingredients together.
-
UNII 1G5HNE09V8
A plant-based ingredient derived from whole corn. It serves as a filler and binder to add bulk and help hold the tablet or capsule together during manufacturing.
5 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesdisteardimonium hectorite, isobutane, kaolin, SD alcohol 40-B, zea mays (corn) starch
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed —
ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.
Manufacturer & labeler
LabelerWinco Foods, LLC
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code67091
First marketedSep 2021
Product typeHuman Otc Drug
Portfolio138 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage
⏱️ Dosage and Administration
⚠️ Warnings
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
📄 Do Not Use
📄 When Using This Product
📄 Stop Use and Ask a Doctor If
📄 Keep Out of Reach of Children
📄 Other Information
📄 Questions or Comments
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Uses cures most athlete's foot (tinea pedis), ringworm (tinea corporis) and jock itch (tinea cruris) relieves symtoms of athlete's foot, including itching, burning and cracking
⏱️ Dosage and Administration ▾
Directions wash affected area and dry thoroughly shake can well and spray a thin layer 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 spaces between toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily use daily for 4 weeks for athlete's foot and ringworm; use daily for 2 weeks for jock itch; if condition persists, consult a doctor this product is not effective on scalp or nails if nozzle clogs, clean with a pin
⚠️ Warnings ▾
Warnings For external use only. Flammable : Do not use while smoking or near heat or flame. Do not puncture or incinerate.
Contents under pressure. Do not store at temperature above 120°F. Intentional misuse by deliberately concentrationg and inhaling contents can be harmful or fatal.
When using this product avoid contact with the eyes or mouth use only as directed Stop use and ask a doctor if irritation occurs no improvement within 4 weeks for athlete's foot and ringworm; 2 weeks for jock itch Do not use on children under 2 years of age unless directed by a doctor. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.
🧪 Active Ingredient ▾
Active ingredient Miconozole nitrate 2%
🧪 Inactive Ingredients ▾
Inactive ingredients disteardimonium hectorite, isobutane, kaolin, SD alcohol 40-B, zea mays (corn) starch
🎯 Purpose ▾
Purpose Antifungal
📄 Do Not Use ▾
Do not use on children under 2 years of age unless directed by a doctor.
📄 When Using This Product ▾
When using this product avoid contact with the eyes or mouth use only as directed
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if irritation occurs no improvement within 4 weeks for athlete's foot and ringworm; 2 weeks for jock itch
📄 Keep Out of Reach of Children ▾
Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.
📄 Other Information ▾
Other infomation store between 20 o and 30 o C (68 o and 86 o F)
📄 Questions or Comments ▾
Questions Call 800-824-1706 Monday - Friday 9 am - 4pm MST
📄 Package Label / Principal Display Panel ▾
PRINCIPAL DISPLAY PANEL Foot Powder Spray Miconazole Nitrate 2%/ ANTIFUNGAL Cures Most Athelete's Foot Relieves Itching, Cracking and Burning Talc Free NET WT
4.6 OZ (130g) miconazole 4
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
About this NDC listing & data coverage
Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope. |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.
Questions about this listing
Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Winco Foods, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Winco Foods, LLC is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
For educational and professional reference only — not medical advice. Pricing reflects published
NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.