Fungi Nail Anti-Fungal Pen Tolnaftate 1 g/100mL Liquid
by Kramer Laboratories · 1 TUBE, WITH APPLICATOR in 1 CARTON (55505-193-51) / 3 mL in 1 TUBE, WITH APPLICATOR
NDC 55505-0193-51
🏷️ FDA NDC (as labeled)
55505-193-51
billing pads the product segment with a zero
This package
Contains3 mL in 1 tube, with applicator
Pack sizes2 compare ↓
Also comes in:
3 mL 55505-0193-60
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)
55505-193-51
Product NDC
55505-193
11-digit billing NDC
55505019351
RxCUI
313423
UNII
06KB629TKV
Application #
M005
SPL Set ID
1a0a3b14-d8f2-4363-b3c9-f5028e8eada3
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2020-03-01
Route
TOPICAL
Dosage form
LIQUID
Substance
TOLNAFTATE
Why two NDCs?
The FDA registers this code as 55505-193-51 — 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 → 55505-0193-51. 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
LabelerKramer Laboratories
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code55505
First marketedMar 2020
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.
🩺 Clinical
📗 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.
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 mL | 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:
3 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.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Maximum Strength Antifungal Liquid 10 mg/mL 00363-2026-01 | Walgreens | 1 bottle | — | — | FDA listed | — |
| Antifungal Liquid 10 mg/mL 00363-4471-01 | Walgreens | 1 bottle | — | — | FDA listed | — |
| Antifungal Liquid Maximum Strength 10 mg/mL 00363-7998-01 | Walgreens | 1 bottle | — | — | FDA listed | — |
| Antifungal Solution Maximum Strength 10 mg/mL 11822-9600-01 | Rite | 1 bottle | — | — | FDA listed | — |
| Meijer Maximum Strength Athletes Foot Antifungal 10 mg/g 23667-0811-01 | Formulated | 150 g | — | — | Discontinued | — |
| Signature Care Athletes Foot Antifungal 10 mg/g 23667-0813-01 | Formulated | 150 g | — | — | Discontinued | — |
| Up and Up Soothing Antifungal 10 mg/g 23667-0816-01 | Formulated | 150 g | — | — | Discontinued | — |
| ProClearz Maximum Strength Fungal Shield Brush-on Antifungal 10 mg/mL 29784-0181-02 | Rooftop | 1 bottle | — | — | FDA listed | — |
| Proclearz Professional Fungal Shield 10 mg/mL 29784-0184-01 | Rooftop | 1 bottle | — | — | FDA listed | — |
| Antifungal Liquid 10 mg/mL 36800-0399-01 | TopCo | 1 bottle | — | — | FDA listed | — |
| CLARUS Antifungal 1 g/100mL 44577-0002-01 | Clinical | 15 ml | — | — | FDA listed | — |
| CLARUS AC Antifungal Solution 10 mg/g 44577-0128-00 | Clinical | 15 g | — | — | FDA listed | — |
| Formula 3 10 mg/mL 49406-0003-15 | The | 1 bottle | — | — | FDA listed | — |
| Formula 7 - The Solution 1 g/100g 49406-0007-15 | The | 15 g | — | — | FDA listed | — |
| Hi Vetic 1 g/100mL 49873-0050-02 | Sato | 1 bottle | — | — | FDA listed | — |
| Silka Antifungal 1 g/100mL 50066-0085-01 | Genomma | 1 bottle | — | — | FDA listed | — |
| Nail Renovar Plus 1 g/100mL 50405-0030-02 | SOHM, | 15 ml | — | — | FDA listed | — |
| CIDACIN Antifungal Treatment 1 g/100mL 51151-0000-01 | Pedicis | 1 bottle | — | — | FDA listed | — |
| Maximum Strength Antifungal Liquid .3 g/30mL 51316-0898-00 | CVS | 30 ml | — | — | FDA listed | — |
| Toe Area Treatment 10 mg/mL 51316-0981-01 | CVS | 1 bottle | — | — | FDA listed | — |
| Fungicure Anti-Fungal Liquid 8.65 mg/mL 52389-0298-30 | Kobayashi | 1 bottle | — | — | FDA listed | — |
| Antifungal Liquid 10 mg/mL 55319-0538-01 | Family | 1 bottle | — | — | FDA listed | — |
| Fungi Nail Toe and Foot 10 mg/mL 55505-0177-26 | Kramer | 1 bottle | — | — | FDA listed | — |
| Fungi Nail Anti-Fungal Pen 1 g/100mLthis 55505-0193-51 | Kramer | 1 tube | — | — | FDA listed | — |
| Opti-Nail 2-in-1 1 g/100mL 55505-0219-67 | Kramer | 5 ml | — | — | FDA listed | — |
| Antifungal Liquid 10 mg/mL 56104-0902-01 | Premier | 1 bottle | — | — | FDA listed | — |
| Mycozyl AL .3 g/30mL 59088-0443-03 | PureTek | 30 ml | — | — | FDA listed | — |
| Micotrin AL .3 g/30mL 59088-0477-03 | PureTek | 30 ml | — | — | FDA listed | — |
| Micomitin Antifungal .3 g/30mL 59088-0640-03 | PureTek | 30 ml | — | — | FDA listed | — |
| Nail Renew 1 g/100mL 62858-0101-51 | Nailrenew | 1 bottle | — | — | FDA listed | — |
| Maximum Strength Antifungal Liquid 10 mg/mL 67091-0753-30 | WinCo | 1 bottle | — | — | FDA listed | — |
| Antifungal Liquid 10 mg/mL 70000-0680-01 | LEADER/Cardinal | 1 bottle | — | — | FDA listed | — |
| Antifungal Liquid 10 mg/mL 70000-0745-01 | LEADER/ | 1 bottle | — | — | FDA listed | — |
| Liquid Antifungal Treatment 10 mg/mL 72446-0012-01 | Hudson | 1 bottle | — | — | FDA listed | — |
| Maximum Strength Antifungal Liquid 10 mg/mL 72446-0013-01 | Hudson | 1 bottle | — | — | FDA listed | — |
| Novonail Solution 1 g/100mL 72839-0507-01 | Derma | 13.3 ml | — | — | FDA listed | — |
| Dermatool Fungal Nail Treatment 1 g/100mL 72839-0510-01 | Derma | 1 bottle | — | — | FDA listed | — |
| Tritolnacide S .01 g/mL 73352-0560-01 | Trifluent | 15 ml | — | — | FDA listed | — |
| Maximum Strength Antifungal Liquid 10 mg/mL 79481-0660-01 | Meijer | 1 bottle | — | — | FDA listed | — |
| Antifungal Liquid 10 mg/mL 79903-0256-30 | Wal-Mart | 1 bottle | — | — | FDA listed | — |
| Antifungal Liquid 10 mg/mL 79903-0394-01 | Wal-Mart | 1 bottle | — | — | FDA listed | — |
| Maximum Strength Antifungal Liquid 10 mg/mL 81522-0077-01 | FSA | 1 bottle | — | — | FDA listed | — |
| Antifungal Liquid 10 mg/mL 82442-0956-01 | Target | 1 bottle | — | — | FDA listed | — |
| Antifungal Liquid 10 mg/mL 82442-0998-01 | Target | 1 bottle | — | — | FDA listed | — |
| Maximum Strength Antifungal Liquid 10 mg/mL 83324-0301-01 | Chain | 1 bottle | — | — | FDA listed | — |
| Toe Fungus 1 g/100mL 83837-0001-01 | Imperial | 75 ml | — | — | FDA listed | — |
| Athletes Foot 1 g/100mL 83837-0002-01 | Imperial | 75 ml | — | — | FDA listed | — |
| Nailtific Nighttime Antifungal Renewal Pen Refill .06 g/6mL 84167-0023-31 | Guangzhou | 1 bottle | — | — | FDA listed | — |
| APUREE Nailtific Extra-Max Strength Nighttime Antifungal 1 g 84167-0479-02 | Guangzhou | 1 vial | — | — | FDA listed | — |
| Nail Lab Fungomer Nailelixir 1 g/100mL 84222-0002-01 | Foshan | 50 ml | — | — | Discontinued | — |
| TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH Liquid 1 g/100mL 84614-0002-01 | Shenzhen | 2 bottles | — | — | FDA listed | — |
| Dermatool Fungal Nail Treatment 1 g/100mL 84728-0510-01 | Papalo | 1 bottle | — | — | FDA listed | — |
| Nekvnro FUNGAL NAIL TREATMENT Kit 1 g/100mL 84844-0019-01 | Guoyu | 2 bottles | — | — | Discontinued | — |
| Ukova Foot Odor Probiotic 1 g/100mL 84867-0011-01 | Jiashen | 30 ml | — | — | FDA listed | — |
| UKVOA Toenail Fungus Treatment 1 g/100mL 84867-0012-01 | Jiashen | 30 ml | — | — | FDA listed | — |
| Alveora NAIL FUNGUS TREATMENT 1 g/100mL 85248-0033-01 | Jiangxi | 30 ml | — | — | FDA listed | — |
| Dermfree Fungi Nail 1 g/100mL 85248-0037-01 | Jiangxi | 15 ml | — | — | FDA listed | — |
| Cndanting Multi-Purpose Nail Repair 1 g/100mL 85248-0040-01 | Jiangxi | 30 ml | — | — | FDA listed | — |
| BeamBalm FUNGL NAIL 1 g/100mL 85248-0047-01 | Jiangxi | 4 ml | — | — | FDA listed | — |
| BeamBalm ANTIFUNGAL NAIL 1 g/100mL 85248-0048-01 | Jiangxi | 11 ml | — | — | FDA listed | — |
| Skapemed Skin Repair 1 g/100mL 85248-0054-01 | Jiangxi | 50 ml | — | — | FDA listed | — |
| Healmusz Fungi Nail 1 g/100mL 85248-0057-01 | Jiangxi | 15 ml | — | — | FDA listed | — |
| HEALMUSZ Multi-PurposeTreatment 1 g/100mL 85248-0058-01 | Jiangxi | 30 ml | — | — | FDA listed | — |
| Reinreude Multi-Purpose Treatment 1 g/100mL 85248-0072-01 | Jiangxi | 30 ml | — | — | FDA listed | — |
| Natuheal Multi -Purpose Treatment 1 g/100mL 85248-0081-01 | Jiangxi | 30 ml | — | — | FDA listed | — |
| Ourui One Fungal Nail Treatment 1 g/100mL 85248-0084-01 | Jiangxi | 2 bottles | — | — | FDA listed | — |
| PUVIDA Helps WITH NAGELPILZ 1 g/100mL 85248-0089-01 | Jiangxi | 2.5 ml | — | — | FDA listed | — |
| FIobow FUNGAL NAIL TREATMENT 1 g/100mL 85248-0095-01 | Jiangxi | 30 ml | — | — | FDA listed | — |
| Serynth Fungi Nail 1 g/100mL 85248-0108-01 | Jiangxi | 15 ml | — | — | FDA listed | — |
| Serynth Helps With Fungal Nail 1 g/100mL 85248-0109-01 | Jiangxi | 2.5 ml | — | — | FDA listed | — |
| Dermfree Helps With Nagelpilz 1 g/100mL 85248-0115-01 | Jiangxi | 4 ml | — | — | FDA listed | — |
| Folupia Fungal Nail Renewal 1 g/100mL 85248-0148-01 | Jiangxi | 30 ml | — | — | FDA listed | — |
| Tolfyra .3 g/30mL 85477-0331-01 | Oncora | 30 ml | — | — | FDA listed | — |
| Nail Fungus Treatment 1 g/100mL 85834-0001-01 | Shenzhen | 30 ml | — | — | Discontinued | — |
| Cureforte Anti Fungal Foot Care 10 mg/mL 85884-0252-02 | STEEL | 1 bottle | — | — | FDA listed | — |
| zourunan MULTI-PURPOS TREATMENT 1 g/100mL 87083-0001-01 | Guchutang | 30 ml | — | — | FDA listed | — |
| Dr. Luke FUNGAL NAIL RENEWAL 1 g/100mL 87147-0005-01 | DANOUS | 30 ml | — | — | Discontinued | — |
| nail fungus treatment 1 mg/100mg 87770-0003-01 | Guangzhou | 30 mg | — | — | FDA listed | — |
| Terramed Just Think Comfort Armor Antifungal Body Wash Citrus 1 g/100mL 83004-0036-01 | Rida | 500 ml | — | — | FDA listed | — |
| Terramed Just Think Comfort Armor Antifungal Body Wash Icy Cool Menthol 1 g/100mL 83004-0037-01 | Rida | 500 ml | — | — | FDA listed | — |
| Terramed Just Think Comfort Armor Antifungal Body Wash Lavender and chamomile 1 g/100mL 83004-0035-01 | Rida | 500 ml | — | — | FDA listed | — |
| MiratiFul Nail Fungus Treatment 1 g/100mL 87885-0001-01 | Texas | 15 ml | — | — | 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
🏛️
2020
On the market since
Mar 2020
📍
2026
Currently FDA-listed
6 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.
🔬 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 Fungi Nail Anti-Fungal Pen (this brand).
Top reported reactions
Reporter sex
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 |
|---|---|---|---|
| 55505-0193-51 You're viewing this | 1 TUBE, WITH APPLICATOR in 1 CARTON (55505-193-51) / 3 mL in 1 TUBE, WITH APPLICATOR | 2020-03-01 | Active |
| 55505-0193-60 | 2 CARTON in 1 PACKAGE (55505-193-60) / 1 TUBE, WITH APPLICATOR in 1 CARTON / 3 mL in 1 TUBE, WITH APPLICATOR | 2021-05-18 | Active |
Pack size FAQ
What quantity is in NDC 55505-0193-51?
NDC 55505-0193-51 is listed by the FDA — 1 tube, with applicator in 1 carton / 3 ml in 1 tube, with applicator.
What NDC number is used to bill for this package of Fungi Nail Anti-Fungal Pen Tolnaftate 1 g/100mL Liquid?
Bill NDC 55505-0193-51 — the 11-digit billing format is 55505019351. 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 | — 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 55505-193-51, 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: 55505-0193-51, written without dashes as 55505019351. 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 55505-0193-51, the first segment (55505) is the labeler code FDA assigned to Kramer Laboratories; the middle segment (0193) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (51) 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 Kramer Laboratories. 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 1 other package presentation of this same product, including 1 tube (55505-0193-60). 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?
Kramer Laboratories 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
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Uses ■ proven 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 ▾
Directions ■ Clean affected area with soap and water and dry thoroughly. ■ Apply a thin layer of Fungi-Nail ® Anti-Fungal over affected area twice daily (morning and night) or as directed by a doctor. ■ Wear well-fitting, ventilated shoes and change shoes and socks at least once daily. ■ For athlete's foot pay special attention to spaces between the toes. ■ For athlete's foot and ringworm, use daily for 4 weeks. ■ To prevent athlete's foot, apply once or twice daily (morning and/or night). ■ For toe fungus: apply around nail and cuticle area. ■ The product is not effective on the scalp or nails. ■ Supervise children in the use of this product.
⚠️ Warnings ▾
Warnings For external use only
📦 Storage and Handling ▾
Other information ■ Store at room temperature 15°-30°C (59°-86°F). Protect from freezing. If freezing occurs warm to room temperature. ■ Keep carton for full product information .
🧪 Active Ingredient ▾
Active Ingredient Purpos e Tolnaftate 1% Anti-fungal
🧪 Inactive Ingredients ▾
Inactive ingredients 3-0-ethyl ascorbic acid, aloe barbadensis leaf juice, cinnamomum zeylanicum bark oil, citric acid, cocos nucifera (coconut) oil, dimethicone, disodium EDTA, DMDM hydantoin, eucalyptol, eugenia caryophyllus (clove) leaf oil, glycerin, glyceryl stearate SE, lavandula angustifolia (lavender) oil, melaleuca alternifolia (tea tree) leaf oil, mineral oil, olea europaea (olive) fruit oil, PEG-100 stearate, phenoxyethanol, potassium sorbate, propylene glycol, sodium benzoate, thymus vulgaris (thyme) oil, titanium dioxide, tocopheryl acetate, water, xanthan gum
🎯 Purpose ▾
Active Ingredient Purpos e Tolnaftate 1% Anti-fungal
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.