HomeNDC LookupIngredientsClotrimazole › 87800-0005-01
MOROVAN RINGWORM TREATMENT Clotrimazole 1 g/100g Cream, 60 g — NDC 87800-0005-01 package photo

MOROVAN RINGWORM TREATMENT Clotrimazole 1 g/100g Cream, 60 g

by HONG KONG UNORDERED TRADING CO., LIMITED · 60 g in 1 BOTTLE (87800-0005-1)
NDC 87800-0005-01
🏷️ FDA NDC (as labeled) 87800-0005-1 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 17, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
Other active recalls for Clotrimazole (different manufacturers) — 2 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0210-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0211-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 87800-0005-1
Product NDC 87800-0005
11-digit billing NDC 87800000501
Application # M005
SPL Set ID 5b56636e-e257-0184-e063-6394a90a0e94
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 2026-09-13
Route TOPICAL
Dosage form CREAM
Substance CLOTRIMAZOLE
Why two NDCs? The FDA registers this code as 87800-0005-1 — a 5-4-1 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 package segment → 87800-0005-01. 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.

🏭 Manufacturer & labeler

LabelerHONG KONG UNORDERED TRADING CO., LIMITED
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code87800
First marketedSep 2026
Product typeHuman Otc Drug
Portfolio7 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
  • It depends on which product you have. The topical creams, solutions, and sprays treat common fungal skin infections — athlete's foot, jock itch, and ringworm. The CLOTIC ear drops...
  • What kinds of infections does clotrimazole actually treat?
  • You may start to notice some relief within a few days, but it's important to finish the full course. For athlete's foot and ringworm, that means using it every day for 4 weeks. For...
  • How long do I need to use it before it starts working?
📖 Read our full Clotrimazole guide →
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 K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • UNII Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • UNII P6YC3EG204
    Cyanocobalamin is a synthetic form of vitamin B12. It's used in medicines as a nutritional ingredient and to help maintain the product's stability and potency over time.
  • UNII 8FP93ED6H2
    Witch hazel is a plant extract made from the leaves and twigs of the witch hazel shrub. In medicines, it works as a soothing and astringent ingredient that helps reduce inflammation and tighten skin.
  • UNII VIF565UC2G
    Tea tree oil is an essential oil extracted from the leaves of the Australian tea tree plant. In medicines, it typically serves as a flavoring agent, fragrance, or antimicrobial component in topical formulations.
  • UNII 1AEY1M553N
    A natural oil extracted from spearmint or field mint leaves, used as a flavoring agent to give medicines a minty taste and aroma. It may also provide a cooling sensation in topical products.
  • UNII L7T10EIP3A
    A cooling compound from mint plants used as a flavoring agent and to create a fresh sensation in medicines. It helps mask bitter tastes and improve how the product feels in the mouth.

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

The official label also statesInactive ingredients MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL, MENTHAHAPLOCALYX OIL, MENTHOL, BUTYROSPERMUM PARKII(SHEA) BUTTER, HAMAMELIS VIRGINIANA (WITCH HAZEL)WATER, CYANOCOBALAMIN, COCOS NUCIFERA (COCONUT) OIL

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 DailyMedingredient 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 systemPer gPer 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

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Rugby Clotrimazole Antifungal Cream 1 g/100g 00536-1265-26 Rugby 1 tube $0.049 Availability likely
Clotrimazole 1 g/100g 70000-0667-01 Cardinal 1 tube $0.063 Availability likely
clotrimazole 1 g/100g 45802-0434-01 Padagis 1 tube $0.146 Discontinued
Clotrimazole 1 g/100g 51672-2002-01 Sun 1 tube $0.185 Availability likely
Terrasil Jock Itch Treatment Maximum Strength 1 g/100g 24909-0214-14 Aidance 14 g FDA listed
TheraPlus Plus 1 g/100g 55621-0003-01 Zhejiang 35 g FDA listed
Clotrimazole 1 g/100g 71205-0434-05 Proficient 1 tube FDA listed
Tagrid Antifungal Jock Itch Cream Non-Steroidal Clotrimazole 1% 1 g/100g 85384-0021-01 TAGRID 60 g FDA listed
Terrasil JockItch Treatment Maximum Strength 1 g/100g 24909-0212-50 Aidance 50 g FDA listed
CVS Antifungal Ringworm 1 g/100g 59779-0514-01 CVS 1 tube FDA listed
Antifungal 1 g/100g 84722-3059-00 VIVE 1 g FDA listed
Tagrid Balanitis Relief 1 g/100g 85384-0018-01 TAGRID 30 g FDA listed
Clotrimazole 1 g/100g 68788-8830-02 Preferred 1 tube FDA listed
Rite Aid antifungal ringworm 1 g/100g 11822-1110-01 Rite 1 tube FDA listed
Terrasil Tinea Treatment MAX 1 g/100g 24909-0104-14 Aidance 14 g Discontinued
Femmesil 1 g/100g 24909-0203-25 Aidance 1 bottle Discontinued
clotrimazole 1 g/100g 63187-0559-15 Proficient 1 tube FDA listed
Tagrid Antifungal Ringworm Treatment 1% CLOTRIMAZOLE 1 g/100g 85384-0006-01 TAGRID 100 g FDA listed
Tagrid Intertrigo Cream For Skin Fold Rash Clotrimazole 1% 1 g/100g 85384-0022-01 TAGRID 56.7 g FDA listed
femmesil Ultra Therapy 1 g/100g 24909-0050-28 Aidance 28 g FDA listed
clotrimazole 1 g/100g 50090-0562-00 A-S 1 tube FDA listed
clotrimazole 1 g/100g 68071-4225-05 NuCare 15 g FDA listed
Clotrimazole 1% 1 g/100g 83324-0041-01 Chain 1 tube FDA listed
ElixirCurozole 1 g/100g 84546-0003-01 ELIXIR 1 tube FDA listed
Rugby Clotrimazole Antifungal Cream 1 g/100g 68788-8901-02 Preferred 1 tube FDA listed
Clotrimazole 1 g/100g 50090-4971-00 A-S 1 tube FDA listed
Hua Tuo Xian Gao Antifungal 1 g/100g 55614-0650-01 MADISON 1 tube FDA listed
PerfectHeal Antifungal 1 g/100g 69070-0303-01 Zhejiang 1 tube FDA listed
Clotrimazole 1 g/100g 69396-0001-04 TRIFECTA 1 tube FDA listed
Clotrimazole 1 g/100g 69396-0087-01 TRIFECTA 1 tube FDA listed
Athletes Foot Cream 1 g/100g 87739-0001-01 Shenzhen 28 g FDA listed
terrasil Antifungal Cleansing Bar 1 g/100g 24909-0037-75 Aidance 75 g FDA listed
Clotrimazole 1 g/100g 63187-0501-15 Proficient 1 tube FDA listed
Clotrimazole 1 g/100g 68788-8216-03 Preferred 1 tube FDA listed
Tagrid Antifungal Clotrimazole 1% 1 g/100g 85384-0019-01 TAGRID 100 g FDA listed
Tagrid Feminine Itch Relief Cream Antifungal Formula Clotrimazole 1% 1 g/100g 85384-0023-01 TAGRID 56.7 g FDA listed
terrasil Folliculitis Cream Maximum Strength 1 g/100g 24909-0064-50 Aidance 50 g FDA listed
Terrasil Ringworm Treatment MAX 1 g/100g 24909-0102-14 Aidance 14 g Discontinued
Terrasil Anti-Fungal Treatment MAX 1 g/100g 24909-0106-14 Aidance 14 g Discontinued
Antifungal 1 g/100g 67777-0727-02 Dynarex 72 tubes FDA listed
Clotrimazole 1 g/100g 50090-6546-00 A-S 1 tube FDA listed
clotrimazole 1 g/100g 68071-3395-03 NuCare 30 g FDA listed
Trimazole 1 g/100g 73352-0570-01 Trifluent 1 tube FDA listed
Kerova ANTIFUNGAL 1 g/100g 85959-0002-01 Guangzhou 100 g FDA listed
Terrasil Athletes Foot AntiFungal Treatment Max 1 g/100g 24909-0207-25 Aidance 25 g Discontinued
clotrimazole 1 g/100g 50090-1770-00 A-S 1 tube FDA listed
Cura Hongo Antifungal 1 g/100g 55758-0102-02 Pharmadel 1 tube Discontinued
Tea Tree Antifungal 1 g/100g 87800-0001-01 HONG 100 g FDA listed
Morovan Ringworm Treatment 1 g/100gthis 87800-0005-01 HONG 60 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

🏛️
2026
On the market since
Sep 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔓
·
Generic versions listed
see equivalents
Generic appears available

FDA-approved generic versions are listed, and recent pricing/market data suggests they may be available — see Therapeutic equivalents.

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 Clotrimazole (matched by generic name) — the program that covers self-administered drugs. 13 manufacturers.
⚠️ 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 Clotrimazole. 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
$6.43M
Claims incl. refills
276K
Beneficiaries
207.9K
Spend / beneficiary
$30.91
Spend / claim
$23.28
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
87800-0005-01 You're viewing this 60 g in 1 BOTTLE (87800-0005-1) 2026-09-13 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 ✓ 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 87800-0005-1, 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: 87800-0005-01, written without dashes as 87800000501. 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 87800-0005-01, the first segment (87800) is the labeler code FDA assigned to HONG KONG UNORDERED TRADING CO., LIMITED; the middle segment (0005) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 HONG KONG UNORDERED TRADING CO., LIMITED. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
HONG KONG UNORDERED TRADING CO., LIMITED 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.
📄 FDA label 19 words

No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.

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.