NDC 11701-0067-14 — Critic Aid Clear AF Miconazole Nitrate 20 mg/g

🆔 Identity & classification

FDA NDC (as labeled) 11701-067-14

Product NDC 11701-067

11-digit billing NDC 11701006714

NCPDP billing unit GM — per gram (weight)

RxCUI 998442, 998450

UNII VW4H1CYW1K

Application # M005

SPL Set ID cbc5d976-850a-476e-b179-b7a5a8675524

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 2009-06-15

Route TOPICAL

Dosage form OINTMENT

Substance MICONAZOLE NITRATE

GPI-14 90154050104210

GPI class Critic-Aid Clear AF

GCN Seq No 047965

GCN 13394

HICL code 003031

Ingredient (HICL) Miconazole Nitrate

HIC1 code Q

Therapeutic class — broad (HIC1) Ear/Eye/Nose/Rectum/Topical/Vagina/Other

HIC2 code Q5

Therapeutic class — intermediate (HIC2) Agents Acting Principally On The Skin

HIC3 code Q5F

Therapeutic class — specific (HIC3) Topical Antifungals

AHFS code 84:04.08.08

AHFS class Azoles (Skin And Mucous Membrane)

FDB label name CRITIC-AID CLEAR AF 2% OINT

FDB brand name Critic-Aid Clear Af

Legend status O — Over-the-counter (OTC) drug or device

Why two NDCs? The FDA registers this code as 11701-067-14 — 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 → 11701-0067-14. 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

LabelerColoplast Corp

FDA applicationM005 (OTC MONOGRAPH DRUG)

Labeler code11701

First marketedJun 2009

Product typeHuman Otc Drug

Portfolio16 products on file

🔎 All NDCs from Coloplast Corp

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

Label name CRITIC-AID CLEAR AF 2% OINT Ingredient Miconazole Nitrate

📗 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?

📖 Read our full Miconazole guide →

Patient education

📘 MedlinePlus patient leaflet ↗

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →

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.

🧪 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 A7E6112E4N
A form of vitamin E used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down, helping maintain stability and shelf life.
UNII M28OL1HH48
Croscarmellose sodium is a plant-based substance derived from cellulose. It acts as a disintegrant, helping tablets and capsules break down quickly in the digestive system so the medicine can be absorbed.
UNII 92RU3N3Y1O
Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
UNII 4T6H12BN9U
Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.

4 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesInactive ingredients cellulose gum, dimethicone, petrolatum, tocopheryl acetate Patent Pending See crimp for lot no. and expiration date Manufactured by: Coloplast A/S DK-3050 Humlebaek, Denmark Distributed by: Coloplast Corp. Minneapolis, MN 55411 U.S.A. 1-800-533-0464 www.us.coloplast.com Product #7572 ©2007, Coloplast Corp. Made in the U.S.A. L7-1349

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.

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.

Try another pack size: 4 g 57 g

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
Miconazole Nitrate 20 mg/g 70677-1000-01	STRATEGIC	1 tube	$0.119	—	Availability likely	—
SUNMARK MICONAZOLE NITRATE antifungal 20 mg/g 49348-0689-72	Strategic	1 tube	$0.122	—	Availability likely	—
Miconazole Nitrate 20 mg/g 51672-2001-01	Sun	1 tube	$0.203	—	Availability likely	—
Critic Aid Clear AF 20 mg/gthis 11701-0067-14	Coloplast	142 g	—	—	FDA listed	—
Green Tetterine 2 g/100g 12258-0241-01	S.S.S.	1 can	—	—	FDA listed	—
White Tetterine 2 g/100g 12258-0242-01	S.S.S.	1 tube	—	—	FDA listed	—
Triple Antifungal 2 g/100g 16864-0040-02	Advantice	1 tube	—	—	FDA listed	—
Medline 2 g/100g 53329-0172-10	Medline	71 g	—	—	FDA listed	—
Antifungal 2 g/100g 84722-3060-00	VIVE	1 g	—	—	FDA listed	—
Miconazole Nitrate 20 mg/g 50090-5607-00	A-S	1 tube	—	—	FDA listed	—
Miconazole Nitrate 20 mg/g 50090-5674-00	A-S	1 tube	—	—	FDA listed	—
Miconazole Nitrate 20 mg/g 84387-0003-01	ALLIED	28.4 g	—	—	FDA listed	—
Tagrid Jock Itch Miconazole Nitrate 2% 20 mg/g 85384-0003-01	TAGRID	100 g	—	—	FDA listed	—
Micatin 20 mg/g 65197-0103-05	WellSpring	14 g	—	—	FDA listed	—
Secura Antifungal Extra Thick 20 mg/g 69740-0329-00	Smith	92 g	—	—	FDA listed	—
Secura Antifungal Greaseless 20 mg/g 69740-0328-00	Smith	57 g	—	—	FDA listed	—
Baza Antifungal 20 mg/g 11701-0045-14	Coloplast	142 g	—	—	FDA listed	—
Miconazole Nitrate 20 mg/g 50090-1071-00	A-S	1 tube	—	—	FDA listed	—
Miconazole Nitrate 20 mg/g 50090-7364-00	A-S	1 tube	—	—	FDA listed	—
CAREALL Miconazole Nitrate 20 mg/g 51824-0078-01	New	28 g	—	—	FDA listed	—
FifthPulse Miconazole Nitrate Cream 1oz 20 mg/g 69571-0016-01	Front	28.4 g	—	—	FDA listed	—
Conazol 20 mg/g 59208-0001-30	Laboratorios	30 g	—	—	FDA listed	—
Fungus Master 20 mg/g 63742-0098-01	Clinical	30 g	—	—	FDA listed	—
FifthPulse Miconazole Nitrate Antifungal 20 mg/g 87525-0004-01	WeCare	1 tube	—	—	FDA listed	—
Miconazole 20 mg/g 68016-0291-01	Chain	1 tube	—	—	FDA listed	—
Desenex Antifungal Foot Cream 20 mg/g 00316-0255-01	Crown	1 tube	—	—	FDA listed	—
Medline 20 mg/g 53329-0256-14	Medline	57 g	—	—	FDA listed	—
HSENJT Antifungal Cream 20 mg/g 87951-0001-01	Huizhou	100 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

🏛️

2009

On the market since

Jun 2009

📍

2026

Currently FDA-listed

17 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.

📊 Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Miconazole 3 (matched by generic name) — the program that covers self-administered drugs. 1 manufacturer.

⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Miconazole 3. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.

Period

Total Part D spend

$35.6K

Claims incl. refills

725

Beneficiaries

649

Spend / beneficiary

$54.91

Spend / claim

$49.15

Trend by period

💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

🔬 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 Critic Aid Clear AF (this brand).

Top reported reactions

Vulvovaginal Burning Sensation242

Vulvovaginal Pain79

Vulvovaginal Pruritus73

Condition Aggravated72

Drug Interaction58

Vulvovaginal Discomfort47

Vaginal Haemorrhage42

Age at onset

Neonate1

Infant3

Child3

Adolescent2

Adult79

Elderly62

Reporter sex

Male · 24%

Female · 76%

Unknown · 0%

Serious outcomes

Hospitalization304

Death85

Life-threatening53

Disabling22

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
11701-0067-14 You're viewing this	142 g in 1 TUBE (11701-067-14)	2009-06-15	Active
11701-0067-22	4 g in 1 PACKET (11701-067-22)	2009-06-15	Active
11701-0067-23	57 g in 1 TUBE (11701-067-23)	2009-06-15	Active

You're viewing the largest of 3 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 11701-0067-14?

NDC 11701-0067-14 contains 142 g — 142 g in 1 tube.

What is the difference between NDC 11701-0067-14 and NDC 11701-0067-22?

Both are Critic Aid Clear AF Miconazole Nitrate 20 mg/g Ointment — the drug itself is identical. NDC 11701-0067-14 is the 142 g package, while NDC 11701-0067-22 is the 4 g package.

What NDC number is used to bill for this package of Critic Aid Clear AF Miconazole Nitrate 20 mg/g Ointment?

Bill NDC 11701-0067-14 — the 11-digit billing format is 11701006714. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 FDA registers it as 11701-067-14, 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: 11701-0067-14, written without dashes as 11701006714. 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 11701-0067-14, the first segment (11701) is the labeler code FDA assigned to Coloplast Corp; the middle segment (0067) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (14) 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 Coloplast Corp. Listing status can change — the directory data on this page refreshes weekly.

Does this product come in other package sizes?

Yes — the FDA directory lists 2 other package presentations of this same product, including 4 g (11701-0067-22), 57 g (11701-0067-23). Each has its own NDC and its own page — see the package list near the top of this page.

Who lists this product with the FDA?

Coloplast Corp 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 14 words ▾

Uses For effective treatment of jock itch. Relieves itching, scaling, irritation, redness and discomfort.

⏱️ Dosage and Administration 55 words ▾

Directions clean the affected area and dry thoroughly apply thin layer of product over affected area twice daily (morning and night), or as directed by a doctor supervise children in the use of this product. Use daily for 2 weeks. If condition persists, consult a doctor. This product is not effective on scalp or nails.

⚠️ Warnings 71 words ▾

Warnings When using this product avoid contact with eyes do not use on children under 2 years of age unless directed by a doctor Stop using this product and ask a doctor if irritation occurs or there is no improvement within 2 weeks. For external use only. Keep this and all drugs out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 5 words ▾

Active ingredient Miconazole nitrate, 2%

🧪 Inactive Ingredients 45 words ▾

Inactive ingredients cellulose gum, dimethicone, petrolatum, tocopheryl acetate Patent Pending See crimp for lot no. and expiration date Manufactured by: Coloplast A/S DK-3050 Humlebaek, Denmark Distributed by: Coloplast Corp. Minneapolis, MN 55411 U.S.A. 1-800-533-0464 www.us.coloplast.com Product #7572 ©2007, Coloplast Corp. Made in the U.S.A. L7-1349

🎯 Purpose 2 words ▾

Purpose Antifungal

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

🔗 Related NDC lookups

🧪 All Miconazole Nitrate NDCsSame ingredient 🏭 All Coloplast labeler NDCsLabeler code 11701 📚 All Azole Antifungal NDCsDrug class

💊 Related drugs in this class

Other drugs that share this product’s specific therapeutic class — Topical Antifungals.

Naftifine Hcl 00115-1510-48 Nystatin/Triamcinolone Acet 00168-0081-15 Oxiconazole Nitrate 00168-0358-30 Tolnaftate 00363-0695-90 Gentian Violet 00395-1003-92 Ciclopirox Olamine 00713-0638-15 Gentian Violet/Brgreen/Proflav 66689-0710-06

Where does this data come from?

Other drugs sharing this product’s First Databank therapeutic class (HIC3). Each links to that NDC’s page in our directory.

Critic Aid Clear AF Miconazole Nitrate 20 mg/g Ointment, 142 g

🆔 Identity & classification

🏷️ RxNorm drug class

🏭 Manufacturer & labeler

🩺 Clinical

Patient education

Supplement & herbal interactions

🧪 Inactive Ingredients / Excipients

Inactive ingredient FAQ

💲 Pricing

🔁 Therapeutic equivalents

⏳ Availability & generic status

📊 Medicare Part D spend CMS · PART D · 2026 (Q1)

🔬 Reported adverse events (FAERS)

Top reported reactions

Age at onset

Reporter sex

Serious outcomes

📦 Packaging — all sizes for this product

Pack size FAQ

🧭 About this NDC listing & data coverage

Questions about this listing

📄 FDA label — Drug Facts FDA SPL

🔗 Related NDC lookups

💊 Related drugs in this class