ProCure Antifungal Miconazole Nitrate 2% 2 g/100g Powder, 85 g
by Twin Med LLC · 85 g in 1 BOTTLE (55681-043-03)
NDC 55681-0043-03
🏷️ FDA NDC (as labeled)
55681-043-03
billing pads the product segment with a zero
OTC
On market
Non-controlled
🗂️ Data synced 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
FDA NDC (as labeled)
55681-043-03
Product NDC
55681-043
11-digit billing NDC
55681004303
RxCUI
998461
UNII
VW4H1CYW1K
UPC
0816516015632
Application #
M005
SPL Set ID
3d375325-ddad-f1e1-e063-6394a90a679f
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
2025-12-01
Route
TOPICAL
Dosage form
POWDER
Substance
MICONAZOLE NITRATE
Why two NDCs?
The FDA registers this code as 55681-043-03 — 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 → 55681-0043-03. 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.
🏷️ 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.
🏭 Manufacturer & labeler
LabelerTwin Med LLC
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code55681
First marketedDec 2025
Product typeHuman Otc Drug
Portfolio48 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.
🩺 Clinical
📗 Our plain-language guide HelloPharmacist
- For a 7-night vaginal cream, you insert one full applicator into your vagina at bedtime for 7 nights in a row. If you have itching or irritation on the outside, squeeze a small amo...
- I bought a miconazole cream for a vaginal yeast infection — how do I use it correctly?
- Yes — topical miconazole creams and powders are specifically made for those conditions. For athlete's foot and ringworm, you'd apply it to clean, dry skin twice a day for 4 weeks....
- Can I use miconazole cream on my skin for athlete's foot or jock itch?
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.
💬 Questions about Miconazole Nitrate 2%?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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.
Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured
IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.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.
💲 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 g | 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.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Miconazorb AF 20 mg/g 46122-0789-29 | AmerisourceBergen | 71 g | $0.058 | — | Availability likely | — |
| Miconazole Nitrate 1.42 g/71g 70000-0323-01 | LEADER/ | 71 g | $0.058 | — | Availability likely | — |
| Antifungal Powder 20 mg/g 70000-0679-01 | LEADER/ | 71 g | $0.058 | — | Availability likely | — |
| Desenex 20 mg/g 00316-0225-15 | Crown | 43 g | — | — | Discontinued | — |
| Zeasorb Athletes Foot 20 mg/g 00316-8000-01 | Crown | 71 g | — | — | FDA listed | — |
| Zeasorb Jock Itch 20 mg/g 00316-8001-02 | Crown | 71 g | — | — | FDA listed | — |
| Foot Powder 20 mg/g 00363-7999-01 | Walgreens | 71 g | — | — | FDA listed | — |
| Jock Itch Powder 20 mg/g 00363-9223-01 | Walgreens | 71 g | — | — | FDA listed | — |
| Miconazole Nitrate Antifungal Powder 2 g/100g 10135-0720-85 | Marlex | 85 g | — | — | FDA listed | — |
| Lotrimin AF Jock Itch 20 mg/g 11523-0150-01 | Bayer | 177 g | — | — | FDA listed | — |
| Lotrimin Antifungal 20 mg/g 11523-0919-01 | Bayer | 90 g | — | — | FDA listed | — |
| Micro-Guard (AF) 20 mg/g 11701-0038-16 | Coloplast | 85 g | — | — | FDA listed | — |
| Anti-Fungal Powder 20 mg/g 30142-0947-71 | The | 71 g | — | — | FDA listed | — |
| Miconazole Nitrate 1.42 g/71g 36800-0385-25 | Topco | 71 g | — | — | FDA listed | — |
| Anti-Fungal Powder 20 mg/g 36800-0613-01 | TopCo | 71 g | — | — | FDA listed | — |
| Miconazole Nitrate 2 g/100g 42291-0938-85 | AvKARE | 85 g | — | — | FDA listed | — |
| Anti-Fungal Powder 20 mg/g 51316-0980-01 | CVS | 71 g | — | — | FDA listed | — |
| Remedy Antifungal 2 g/100g 53329-0169-79 | Medline | 85 g | — | — | FDA listed | — |
| Miconazole Nitrate 20 mg/g 53943-0976-01 | Discount | 71 g | — | — | FDA listed | — |
| ProCure Antifungal 2 g/100gthis 55681-0043-03 | Twin | 85 g | — | — | FDA listed | — |
| Anti- Fungal Miconazole Nitrate 1.42 g/71g 56104-0253-01 | Premier | 71 g | — | — | FDA listed | — |
| Anti-fungal Powder Miconazole Nitrate 20 mg/g 56104-0500-00 | Premier | 71 g | — | — | FDA listed | — |
| Medicated Athletes Foot Powder 20 mg/g 56104-0906-01 | Premier | 99 g | — | — | FDA listed | — |
| Mycozyl AP 2 g/85g 59088-0442-07 | PureTek | 85 g | — | — | FDA listed | — |
| Micotrin AP 2 g/85g 59088-0478-07 | PureTek | 85 g | — | — | FDA listed | — |
| 1236-CS Antifungal Powder (Talc Free) 20 mg/g 67777-0313-04 | Dynarex | 24 bottles | — | — | FDA listed | — |
| THERA Antifungal Body 20 mg/g 68599-0207-03 | McKesson | 85 g | — | — | FDA listed | — |
| GeriGentle Miconazole nitrate 2 g/100g 69771-0165-03 | GERI-GENTLE | 85 g | — | — | FDA listed | — |
| Miconazole Nitrate 1.42 g/71g 69842-0490-25 | CVS | 71 g | — | — | FDA listed | — |
| Miconazole Nitrate 1.42 g/71g 72446-0007-71 | Hudson | 71 g | — | — | FDA listed | — |
| Miconazole Nitrate 20 mg/g 72446-0014-01 | Hudson | 71 g | — | — | FDA listed | — |
| DCH Labs Antifungal Jock 2 g/100g 72839-0096-02 | Derma | 71 g | — | — | FDA listed | — |
| Warrior Antifungal Foot 2 g/100g 72839-0961-02 | Derma | 71 g | — | — | FDA listed | — |
| Anti-fungal Powder Miconazole Nitrate 20 mg/g 79481-0621-01 | Meijer | 71 g | — | — | FDA listed | — |
| Antifungal 20 mg/g 80513-0771-03 | Advanced | 85 g | — | — | FDA listed | — |
| Evercare Antifungal Treatment Super Absorbent Powder 20 mg/g 83099-0000-00 | PANEFFORT, | 85 g | — | — | FDA listed | — |
| Dermachange Jock 2 g/100g 83520-0961-02 | Private | 71 g | — | — | FDA listed | — |
| Happy Nuts Jock Itch Powder 2 g/100g 87151-0111-01 | Suit | 71 g | — | — | FDA listed | — |
| Antifungal Powder 2 g/100g 87236-0012-03 | Aldermed | 85 g | — | — | FDA listed | — |
| Claravie 2 g/100g 61554-0316-11 | Gentell | 85 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.
⏳ Availability & generic status
🏛️
2025
On the market since
Dec 2025
📍
2026
Currently FDA-listed
1 year 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.
🔬 Reported adverse events (FAERS)
Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for ProCure Antifungal (this brand).
Top reported reactions
Reporter sex
Male · 67%
Female · 33%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 55681-0043-03 You're viewing this | 85 g in 1 BOTTLE (55681-043-03) | 2025-12-01 | Active |
🧭 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 | — Not published for this NDC No photo available yet for this listing. |
| Inactive ingredients (structured) | — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 FDA registers it as 55681-043-03, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 55681-0043-03, written without dashes as 55681004303. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 55681-0043-03, the first segment (55681) is the labeler code FDA assigned to Twin Med LLC; the middle segment (0043) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (03) identifies this exact package size and type. Together they name one specific package of one specific product.
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 Twin Med LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Twin Med 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.
📄 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
🎯 Indications and Usage ▾
Uses Uses Proven clinically effective in the treatment of most athlete’s foot, jock itch and ringworm Relieves itching, scaling, cracking, burning, redness, soreness, irritation, and discomforts associated with all three treatments. Also relieves chaffing associated with jock itch.
⏱️ Dosage and Administration ▾
Directions Directions clean affected area and dry thoroughly apply thin layer of powder to 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 space between the toes; wear well-fitting, ventilated shoes and change shoes and socks at least 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 ▾
Warnings Warnings For external use only 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 eyes Stop using and ask a doctor if Stop using and ask a doctor if irritation occurs there is no improvement within 4 weeks (for athlete’s foot or ringworm) or 2 weeks (for jock itch) Keep out of reach of children Keep out of reach of Children . In case of accidental ingestion, contact a physician or Poison Control Center right away.
🧪 Active Ingredient ▾
Active Ingredient Mconazole Nitrate 2%
🧪 Inactive Ingredients ▾
Inactive Ingredients Inactive Ingredients: Colloidal Silicon Dioxide, Corn Starch, Dipotassium Glycyrrhizinate, Sodium Benzoate
🎯 Purpose ▾
Purpose Antifungal
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 ↗
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.