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Tagrid Athlete Foot Antifungal with Tolnaftate 1 g/100mL Spray, 50 mL — NDC 85384-0017-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Tagrid Athlete Foot Antifungal with Tolnaftate 1 g/100mL Spray, 50 mL — NDC 85384-0017-2 (Billing 85384-0017-02)

by TAGRID LLC · 50 mL in 1 BOTTLE, SPRAY

This is a package of 50 mL of Tagrid Athlete Foot Antifungal with Tolnaftate 1 g/100mL Spray from TAGRID LLC, marketed since Aug 2025 and currently FDA-listed.

NDC 85384-0017-02
🏷️ FDA NDC (as labeled) 85384-0017-2 billing pads the package segment with a zero
This package
Contains50 mL Pack sizes3 compare ↓
Product page 85384-0017-01 Also comes in: 30 ml 85384-0017-3 100 ml 85384-0017-1
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 85384-0017-2
Product NDC 85384-0017
11-digit billing NDC 85384001702
Application # M016
SPL Set ID d3c514e7-9913-4f8d-87ff-777563bec237
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-08-10
Route TOPICAL
Dosage form SPRAY
Substance TOLNAFTATE
Why two NDCs? The FDA registers this code as 85384-0017-2 — 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 → 85384-0017-02. 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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • It treats fungal skin infections like athlete's foot, ringworm and, in some products, jock itch. Many products also help prevent athlete's foot. Some are made for skin around the n...
  • Wash and dry the area well, then apply a thin layer. Most products are used twice a day, morning and night. The length of use varies, often 4 weeks for athlete's foot and ringworm,...
  • The main one is skin irritation. If that happens, stop using it and talk to a doctor.
  • Call if you see no improvement within 4 weeks for athlete's foot or ringworm, or 2 weeks for jock itch. Call if irritation develops. Call right away if anyone swallows it.
📖 Read our full Tolnaftate 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.

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 mLPer 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: 30 ml 100 ml
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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
85384-0017-01 85384-0017-1 Main listing 100 mL in 1 BOTTLE, SPRAY 2025-08-10 — Active
85384-0017-02 You're viewing this 50 mL in 1 BOTTLE, SPRAY 2025-08-10 — Active
85384-0017-03 85384-0017-3 30 mL in 1 BOTTLE, SPRAY 2025-08-10 — Active

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

Pack size FAQ

What quantity is in this package?
This package contains 50 mL — 50 ml in 1 bottle, spray.
How does this package differ from NDC 85384-0017-03?
Both are Tagrid Athlete Foot Antifungal with Tolnaftate 1 g/100mL Spray — the drug itself is identical. This page's package is the 50 mL one, while NDC 85384-0017-03 is the 30 ml package.
What NDC number is used to bill for this package of Tagrid Athlete Foot Antifungal with Tolnaftate 1 g/100mL Spray?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Athletes Foot 10 mg/g 00536-1481-01 Rugby 130 g $0.033 — Availability likely —
Walgreens Athletes Foot 1 g/100g 00363-0155-05 Walgreens 150 g — — FDA listed —
Tinactin 10 mg/g 11523-0165-03 Bayer 150 g — — FDA listed —
Tolnaftate 1.5 g/150g 11822-0780-05 Rite 150 g — — FDA listed —
Tolnaftate 1.5 g/150g 21130-0213-00 Better 150 g — — FDA listed —
GoodSense Athletes Foot Antifungal 10 mg/g 23667-0803-01 Formulated 150 g — — Discontinued —
CVS Health Antifungal Anthletes Foot 10 mg/g 23667-0805-01 Formulated 150 g — — Discontinued —
SmartSense Maximum Strength Athletes Foot Relief antifungal 10 mg/g 23667-0815-01 Formulated 150 g — — Discontinued —
Good Neighbor Pharmacy Maximum Strength Athletes Foot Relief Antifungal 10 mg/g 23667-0820-01 Formulated 150 g — — Discontinued —
ProClearz Laser Antifungal 10 mg/g 29784-0183-01 Rooftop 85 g — — FDA listed —
Tolnaftate 1.5 g/150g 36800-0006-53 Topco 150 g — — FDA listed —
Tolnaftate 10 mg/g 42507-0415-01 HY-VEE, 150 g — — FDA listed —
Relispray Antifungal Liquid .01 g/g 46063-0810-12 Midas-Care 128 g — — FDA listed —
Antifungal Foot 1 g/100g 52000-0418-03 Universal 103 g — — FDA listed —
Tolnaftate 1.5 g/150g 55301-0131-53 ARMY 150 g — — FDA listed —
HC Max Anti-Fungal 1.5 g/150g 55505-0195-62 Kramer 150 g — — FDA listed —
Tolnaftate 1.5 g/150g 56104-0001-02 Premier 150 g — — Discontinued —
Tolnaftate 1.5 g/150g 63868-0798-53 Chain 150 g — — FDA listed —
Antifungal Liquid 1.5 g/150g 63941-0564-01 VALU 150 g — — FDA listed —
Tolnaftate 1.5 g/150g 67091-0391-05 Winco 150 g — — FDA listed —
Tolnaftate 1.5 g/150g 69256-0034-53 Harris 150 g — — FDA listed —
Tolnaftate 1.5 g/150g 69842-0185-53 CVS 150 g — — FDA listed —
Dr. Scholls Instant Cool Athletes foot treatment with Menthol 10 mg/g 73469-0691-01 Scholl's 150 g — — FDA listed —
Tolnaftate 1.5 g/150g 79481-0591-01 Meijer 150 g — — FDA listed —
Tolnaftate 10 mg/g 79481-0625-01 Meijer 150 g — — FDA listed —
Tolnaftate 1.5 g/150g 79903-0015-53 Wal-Mart 150 g — — FDA listed —
Tolnaftate 10 mg/g 81522-0068-01 FSA 150 g — — FDA listed —
Tolnaftate 10 mg/g 82442-0203-01 Target 150 g — — FDA listed —
Tolnaftate 10 mg/g 83324-0237-53 Chain 150 g — — FDA listed —
Alveora FOOT ODOR PROBIOTIC 1 g/100mL 85248-0030-01 Jiangxi 100 ml — — FDA listed —
Healmusz Foot Odor Probiotic 1 g/100mL 85248-0059-01 Jiangxi 100 ml — — FDA listed —
Serynth Multi-Purpose Funcus 1 g/100mL 85248-0133-01 Jiangxi 100 ml — — FDA listed —
IraEvanes ANTIFUNGAL FOOT 1 g/100mL 85248-0170-01 Jiangxi 118 ml — — FDA listed —
Vamy ANTIFUNGAL 1 g/100mL 85248-0176-01 Jiangxi 100 ml — — FDA listed —
Tagrid Jock Itch 10 mg/mL 85384-0009-01 TAGRID 100 ml — — FDA listed —
Tagrid Athlete Foot Antifungal with Tolnaftate 1 g/100mLthis 85384-0017-02 TAGRID 50 ml — — FDA listed —
Lavinso Athlete Foot 10 mg/mL 87011-0101-02 Lavinso 1 bottle — — Discontinued —
zourunan FOOT ODOR PROBIOTIC 1 g/100mL 87083-0004-01 Guchutang 100 ml — — FDA listed —
BeamBalm ANTIFUNGAL FOOT CARE Spary 1 g/100mL 87786-0005-01 Wenzhou 100 ml — — Discontinued —
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
Aug 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.

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 32MP823R8S
    A plant-derived ingredient from mugwort root, used in traditional herbal formulations. It may function as a flavoring agent, botanical extract, or natural additive in the medicine.
  • UNII 04W97Z676Y
    A plant-derived natural substance from Bassia scoparia fruit used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping in the tablet or capsule.
  • UNII P0M7O4Y7YD
    A plant extract from calendula flowers, traditionally used in formulations. It typically serves as a botanical ingredient that may provide color, fragrance, or skin-conditioning properties to topical products.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII 6FO62KCQ7A
    Disodium hydrogen citrate is a salt derived from citric acid. It acts as a buffer to maintain the pH of the medicine and may also help improve the stability and taste of the product.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 610T51U707
    A plant extract from Canadian mint leaves used to add flavor and aroma to medicines. It helps mask bitter or unpleasant tastes in oral formulations.
  • UNII PBG27B754G
    Phellodendron amurense bark is a plant-derived ingredient from the cork tree. It functions as a natural preservative and antimicrobial agent to help maintain product stability and prevent microbial growth.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 7YC686GQ8F
    A synthetic oily substance made from castor oil. It works as a solubilizer and emulsifier to help mix oily and water-based ingredients together in the medicine.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • 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 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 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

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

The official label also statesInactive ingredients: Water Artemisia vulgaris extract Kochia scoparia fruit extract Dictamnus dasycarpus root extract Smilax glabra root extract Solidago decurrens fruiting top extract Phellodendron amurense bark extract Euphorbia fischeriana root extract Gleditsia sinensis fruit extract Stemona tuberosa root extract

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.

Manufacturer & labeler

LabelerTAGRID LLC
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code85384
First marketedAug 2025
Product typeHuman Otc Drug
Portfolio26 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 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 33 words ▾

Uses: Proven clinically effective in the treatment of most athlete’s foot (tinea pedis) and ringworm (tinea corporis). Helps prevent most athlete’s foot with daily use. For effective relief of itching, burning, and cracking.

⏱️ Dosage and Administration 47 words ▾

Directions: Clean the affected area and dry thoroughly. Spray a thin layer over affected area twice daily (morning and night). For athlete’s foot: pay special attention to the spaces between the toes; wear well-fitting, breathable shoes, and change socks daily. Allow shoes to dry out between uses.

⚠️ Warnings 106 words ▾

For external use only. Avoid contact with eyes, mouth, or mucous membranes. Do not apply to broken or irritated skin.

Flammable: Keep away from heat and flame. Do not use: On children under 2 years of age unless directed by a doctor. For diaper rash.

When using this product Avoid contact with eyes. Use only as directed. If irritation occurs, stop use and consult a doctor.

Stop use and ask a doctor if Condition worsens or does not improve within 2 weeks. Excessive irritation or burning occurs. Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 4 words ▾

Active ingredient: Tolnaftate 1%

🧪 Inactive Ingredients 39 words ▾

Inactive ingredients: Water Artemisia vulgaris extract Kochia scoparia fruit extract Dictamnus dasycarpus root extract Smilax glabra root extract Solidago decurrens fruiting top extract Phellodendron amurense bark extract Euphorbia fischeriana root extract Gleditsia sinensis fruit extract Stemona tuberosa root extract

🎯 Purpose 1 words ▾

Antifungal

📄 Do Not Use 18 words ▾

Do not use: On children under 2 years of age unless directed by a doctor. For diaper rash.

📄 When Using This Product 21 words ▾

When using this product Avoid contact with eyes. Use only as directed. If irritation occurs, stop use and consult a doctor.

📄 Stop Use and Ask a Doctor If 21 words ▾

Stop use and ask a doctor if Condition worsens or does not improve within 2 weeks. Excessive irritation or burning occurs.

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Other Information 17 words ▾

Store between 20°C to 25°C (68°F to 77°F). Avoid excessive heat and direct sunlight. Protect from freezing.

📄 Questions or Comments 7 words ▾

Questions or comments? Contact us at [email protected]

📄 Package Label / Principal Display Panel 31 words ▾

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL Available in 100 mL, 50 mL and 30 mL can. All packages look the same externally, with the only variation being fill volume. package box Can tag

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 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 2 other package presentations of this same product, including 30 ml (85384-0017-03), 100 ml (85384-0017-01). 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.
← 85384-0016-01 · TAGRID 85384-0018-01 · TAGRID →
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.