Tagrid Antifungal Tolnaftate 10 mg/g Soap, 124.74 g
by TAGRID LLC · 124.74 g in 1 BOX (85384-0013-3)
NDC 85384-0013-03
🏷️ FDA NDC (as labeled)
85384-0013-3
billing pads the package segment with a zero
This package
Contains124.74 g
Pack sizes4 compare ↓
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)
85384-0013-3
Product NDC
85384-0013
11-digit billing NDC
85384001303
RxCUI
1807715
UNII
06KB629TKV
Application #
M005
SPL Set ID
7aa42827-59c2-4926-a3a2-e60dd219eb41
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2025-06-09
Route
TOPICAL
Dosage form
SOAP
Substance
TOLNAFTATE
Why two NDCs?
The FDA registers this code as 85384-0013-3 — 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 → 85384-0013-03. 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 Other antifungals for topical use class.
Drug family (ATC)
Other antifungals for topical use
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
LabelerTAGRID LLC
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code85384
First marketedJun 2025
Product typeHuman Otc Drug
Portfolio24 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
📖 What it is MedlinePlus · NLM
Tolnaftate stops the growth of fungi that cause skin infections, including athlete's foot, jock itch, and ringworm. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
Read the full MedlinePlus article ↗📗 Our plain-language guide HelloPharmacist
- It depends on what you're treating. For athlete's foot and ringworm, plan on using it daily for about 4 weeks. For jock itch, 2 weeks is the usual course. Some products mention you...
- How long does it take for tolnaftate to work?
- Tolnaftate is not effective for treating infections on the scalp or on the nails themselves — most products say so right on the label. Some liquid and patch products are designed t...
- Stop applying the product and let your doctor know. A little initial sensitivity can happen, but worsening irritation is a sign that you should get it checked out. Don't push throu...
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Tolnaftate — tap one for details:
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 Tolnaftate?
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.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII V1IA3S3CUS
A plant extract derived from Cnidium monnieri fruit, commonly used in traditional Asian medicine preparations. In formulations, it may serve as an active botanical ingredient or flavoring agent, though its specific role depends on the product type.
-
UNII LA97176ILS
A plant-derived ingredient from the root bark of Dictamnus dasycarpus. It may function as a natural extract or traditional ingredient to support formulation stability or consistency in herbal preparations.
-
UNII 2R04ONI662
Eucalyptus oil is a fragrant liquid extracted from eucalyptus tree leaves. It's used in medicines as a flavor, scent, or soothing agent in topical products and cough preparations.
-
UNII A6W0J6UO7Q
A plant-derived extract from the fruit of the Chinese honey locust tree. It serves as a natural thickener and emulsifier to help blend ingredients and create a smooth, uniform texture in medicines.
-
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 J1BO4MHT2L
A plant material from Canadian mint that provides flavor and aroma to the medicine. It's used to improve taste and make the product more pleasant to take.
-
UNII 8PI54V663Y
Oatmeal is ground oat grain used as a natural filler and texture agent in medicines. It absorbs moisture, adds bulk to the formulation, and may help create a soothing base in topical products.
-
UNII QKA3ZK8IIE
Phellodendron chinense whole is a plant-derived ingredient used in some formulations as a natural binder and filler. It helps hold tablet or capsule ingredients together and add bulk to the final product.
-
UNII IYR6K8KQ5K
A plant extract from sophora flavescens root used as a natural colorant and flavoring agent in medicines. It may also help preserve the product and provide texture.
-
UNII 80N0P0DD9J
A plant-derived ingredient from Stellera chamaejasme used in traditional medicine formulations. It may serve as a natural extract or botanical component in the preparation.
-
UNII EKG8030U4N
A plant-derived ingredient from the Stemona sessilifolia root. It may be used as a natural binder or thickening agent to help hold tablet or capsule ingredients together and improve product texture.
11 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesIngredients: GLEDITSIA SINENSIS FRUIT MENTHA CANADENSIS WH LE STELLERA CHAMAEJASME WHOLE OATMEAL SOPHORA FLAVESCENS ROOT PHELLODENDRON CHINENSE WHOLE CNIDIUM MONNIERI FRUIT STEMONA SESSILIFOLIA ROOT EUCALYPTUS GLOBULUS LEAF OIL DICTAMNUS DASYCARPUS ROOT BARK MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF 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 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 each | 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
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 |
|---|---|---|---|---|---|---|
| Tolnaftate Antifungal 10 mg/g 24385-0032-03 | Amerisource | 1 tube | $0.122 | — | Availability likely | — |
| sunmark antifungal 10 mg/g 49348-0155-29 | Strategic | 1 tube | $0.152 | — | Availability likely | — |
| Inlifay ANTIFUNGAL 1 g/100g 60771-0040-01 | Guangzhou | 232 g | — | — | FDA listed | — |
| Defense Antifungal Medicated Bar 1 g/100g 70856-3581-02 | Defense | 1 not | — | — | FDA listed | — |
| Terramed Just Think Comfort Armor Antifungal Medicated 1 g/100g 83004-0017-01 | Rida | 120 g | — | — | FDA listed | — |
| Quali Life ANTIFUNGAL PERSIMMON 1 g/100g 83566-0606-01 | Guangdong | 300 g | — | — | FDA listed | — |
| Quali Life ANTIFUNGAL CHARCOAL 1 g/100g 83566-0607-01 | Guangdong | 300 g | — | — | FDA listed | — |
| Inlifay ANTIFUNGAL 1 g/100g 83566-0609-01 | Guangdong | 232 g | — | — | FDA listed | — |
| Tagrid Antifungal 10 mg/g 85384-0010-01 | TAGRID | 142 g | — | — | FDA listed | — |
| Tagrid Antifungal 10 mg/gthis 85384-0013-03 | TAGRID | 124.74 g | — | — | FDA listed | — |
| Athlete Foot Medicated bar 1 g/100g 85398-0007-01 | Beautivity | 232 g | — | — | FDA listed | — |
| Hermon Antifungal Soap. 10 mg/g 85398-0019-02 | Beautivity | 226 g | — | — | FDA listed | — |
| Hermon Antifungal Soap. 4 packs 10 mg/g 85398-0020-02 | Beautivity | 452 g | — | — | FDA listed | — |
| Hermon Antifungal .soap. 10 mg/g 85398-0025-02 | Beautivity | 226 g | — | — | FDA listed | — |
| Hermon Antifungal Cleansing Bar 4.52 g/452g 85398-0029-01 | Beautivity | 452 g | — | — | FDA listed | — |
| Hermon Jock Itch Antifungal Treatment .Soap. Bar 1.13 g/113g 85398-0031-01 | Beautivity | 113 g | — | — | FDA listed | — |
| Antifungal Medicated Bar 10 mg/g 85424-0001-01 | RoyceDerm | 232 g | — | — | FDA listed | — |
| ProBliva Antifungal Scrub .soap. Bar 1.13 g/113g 85464-0007-01 | CAVTECH | 113 g | — | — | FDA listed | — |
| Lavinso Antifungal 1 g/100g 87011-0102-01 | Lavinso | 232 g | — | — | Discontinued | — |
| Tea Tree Oil Antifungal Soaps .7 g/70g 87257-0001-01 | Nanjing | 70 g | — | — | FDA listed | — |
| sunmark antifungal 10 mg/g 50090-3358-00 | A-S | 1 tube | — | — | FDA listed | — |
| Thera plus Antifungal Tolnaftate 10 mg/g 80684-0040-01 | FOURSTAR | 1 tube | — | — | FDA listed | — |
| AVON HeXashield Athletes Foot Cream 10 mg/g 43136-0104-01 | Tai | 1 tube | — | — | FDA listed | — |
| equate Athletes Foot 10 mg/g 49035-0499-03 | Wal-Mart | 1 tube | — | — | FDA listed | — |
| Hongo Killer 10 mg/g 58593-0286-01 | Efficient | 1 tube | — | — | FDA listed | — |
| Family Care Antifungal 10 mg/g 65923-0021-28 | United | 1 tube | — | — | FDA listed | — |
| Tolnaftate Cream 1% 10 mg/g 68016-0152-01 | Pharmacy | 1 tube | — | — | FDA listed | — |
| Athletes Foot 10 mg/g 70084-0510-01 | Quantum, | 1 tube | — | — | FDA listed | — |
| Tagrid Athletes Foot Treament 10 mg/g 85384-0008-01 | TAGRID | 100 g | — | — | FDA listed | — |
| Derman antifungal cream 10 mg/g 81929-0004-01 | Taisho | 1 tube | — | — | FDA listed | — |
| TheraCare Antifungal Cream 10 mg/g 71101-0017-01 | Veridian | 1 tube | — | — | FDA listed | — |
| meijer antifungal 10 mg/g 41250-0499-01 | Meijer | 1 tube | — | — | FDA listed | — |
| Family Wellness Athletes Foot Tolnaftate 1 Cream 10 mg/g 55319-0991-00 | Family | 1 tube | — | — | FDA listed | — |
| Tolnaftate 10 mg/g 68071-4245-05 | NuCare | 14.18 g | — | — | FDA listed | — |
| CVS Health Athletes Foot 10 mg/g 69842-0336-14 | CVS | 1 tube | — | — | FDA listed | — |
| Dr.Scholl s Odor X Athlete s Foot 10 mg/g 73469-0618-01 | Scholl's | 1 bottle | — | — | FDA listed | — |
| Tinactin 10 mg/g 11523-0934-02 | Bayer | 1 tube | — | — | FDA listed | — |
| Tolnaftate 10 mg/g 11527-0051-40 | Sheffield | 1 tube | — | — | FDA listed | — |
| Signature Care Antifungal Cream Tolnaftate 1% 10 mg/g 21130-0887-14 | BETTER | 1 tube | — | — | FDA listed | — |
| Winco Foods Tolnaftate 10 mg/g 67091-0276-28 | Winco | 1 tube | — | — | FDA listed | — |
| Tinactin 10 mg/g 11523-1190-01 | Bayer | 1 tube | — | — | FDA listed | — |
| CLARUS Antifungal 10 mg/g 44577-0470-00 | Clinical | 1 tube | — | — | FDA listed | — |
| Natureplex Tolnaftate Antifungal 10 mg/g 67234-0032-01 | Natureplex, | 1 tube | — | — | FDA listed | — |
| CAREALL Tolnaftate 10 mg/g 51824-0001-01 | New | 28 g | — | — | FDA listed | — |
| DG Health Athletes Foot 10 mg/g 55910-0027-28 | Dolgencorp, | 1 tube | — | — | 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
Jun 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 Tagrid Antifungal (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 50%
Female · 50%
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 |
|---|---|---|---|
| 85384-0013-01 | 113.4 g in 1 BOX (85384-0013-1) | 2025-06-09 | Active |
| 85384-0013-02 | 226.8 g in 1 BOX (85384-0013-2) | 2025-12-09 | Active |
| 85384-0013-03 You're viewing this | 124.74 g in 1 BOX (85384-0013-3) | 2025-06-09 | Active |
| 85384-0013-04 | 249.48 g in 1 BOX (85384-0013-4) | 2025-12-09 | Active |
Pack size FAQ
What quantity is in NDC 85384-0013-03?
NDC 85384-0013-03 contains 124.74 g — 124.74 g in 1 box.
What is the difference between NDC 85384-0013-03 and NDC 85384-0013-01?
Both are Tagrid Antifungal Tolnaftate 10 mg/g Soap — the drug itself is identical. NDC 85384-0013-03 is the 124.74 g package, while NDC 85384-0013-01 is the 113.4 g package.
What NDC number is used to bill for this package of Tagrid Antifungal Tolnaftate 10 mg/g Soap?
Bill NDC 85384-0013-03 — the 11-digit billing format is 85384001303. 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 85384-0013-3, 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: 85384-0013-03, written without dashes as 85384001303. 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 85384-0013-03, the first segment (85384) is the labeler code FDA assigned to TAGRID LLC; the middle segment (0013) 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 TAGRID LLC. 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 3 other package presentations of this same product, including 113.4 g (85384-0013-01), 226.8 g (85384-0013-02), 249.48 g (85384-0013-04). 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?
TAGRID 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
🎯 Indications and Usage ▾
Uses For effective treatment of jock itch, ringworm, athlete's foot, folliculitnost tinea For effective relief of itching, burning, and cracking sking skin.
⏱️ Dosage and Administration ▾
DIRECTIONS Wash the affected area well and let the product sit for 1-2 minutes before rinsing. Ensure thorough drying of the affected area. Supervise children when using this product.
For patients seeking immediate relief or experiencing severe symptoms, we recommend applying the ointment. Please note the potential burning and stinging sensation after application, primarily due to menthol and other natural ingredients. Endure any discomfort for 5-10 minutes before experiencing immediate relief.
Use 1-2 times daily for 4 weeks. If the condition persists longer, consult a doctor.
⚠️ Warnings ▾
For external use only Do not use on children under 2 years of age exceptunder the advice and supervision of a doctor. When using this product avoid contact with the eyes. Stop use and ask a doctor if irritation occurs or if there is no improvement within 2weeks for jock itch. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
🧪 Active Ingredient ▾
Tolnaftate
🧪 Inactive Ingredients ▾
Ingredients: GLEDITSIA SINENSIS FRUIT MENTHA CANADENSIS WH LE STELLERA CHAMAEJASME WHOLE OATMEAL SOPHORA FLAVESCENS ROOT PHELLODENDRON CHINENSE WHOLE CNIDIUM MONNIERI FRUIT STEMONA SESSILIFOLIA ROOT EUCALYPTUS GLOBULUS LEAF OIL DICTAMNUS DASYCARPUS ROOT BARK MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL
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.