Hongo Killer Tolnaftate 10 mg/g Cream, 28 g
by Efficient Laboratories Inc · 28 g in 1 TUBE (58593-286-22)
NDC 58593-0286-22
🏷️ FDA NDC (as labeled)
58593-286-22
billing pads the product segment with a zero
This package
Contains28 g
Pack sizes4 compare ↓
OTC
Discontinued
Non-controlled
⚠ Discontinued by firm
🗂️ 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 →
⚠️
Excluded from the active FDA NDC Directory.
The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory.
Search the FDA NDC Directory ↗
🆔 Identity & classification
FDA NDC (as labeled)
58593-286-22
Product NDC
58593-286
11-digit billing NDC
58593028622
UNII
06KB629TKV
Application #
M005
SPL Set ID
5a8bb110-2687-4e29-a771-2362d7726701
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
Discontinued
FDA listing status
Discontinued by firm
Marketing start
2000-01-01
Route
TOPICAL
Dosage form
CREAM
Substance
TOLNAFTATE
Why two NDCs?
The FDA registers this code as 58593-286-22 — 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 → 58593-0286-22. 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
LabelerEfficient Laboratories Inc
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code58593
First marketedJan 2000
Product typeHuman Otc Drug
Portfolio17 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.
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 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
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 |
|---|---|---|---|---|---|---|
| CR-371059 Tolnaftate 1% Cream 1 g/100g 00536-1315-43 | Rugby | 1 g | $0.091 | — | Availability likely | — |
| Tolnaftate Antifungal 10 mg/g 24385-0032-03 | Amerisource | 1 tube | $0.122 | — | Availability likely | — |
| Tolnaftate Cream 1% ANTIFUNGAL 1 g/100g 70000-0084-01 | CARDINAL | 1 tube | $0.122 | — | Availability likely | — |
| sunmark antifungal 10 mg/g 49348-0155-29 | Strategic | 1 tube | $0.152 | — | Availability likely | — |
| Tolnaftate Antifungal 1 g/100g 51672-2020-01 | Sun | 1 tube | $0.152 | — | Availability likely | — |
| Tolnaftate Antifungal 1 g/100g 70677-1001-01 | STRATEGIC | 1 tube | $0.152 | — | Availability likely | — |
| Odor-Eaters Athletes Foot 1 g/100g 10157-3100-01 | Blistex | 1 tube | — | — | FDA listed | — |
| Mentholatum Heel Revival Cream 10 mg/g 10742-0020-01 | The | 1 tube | — | — | FDA listed | — |
| Tinactin 10 mg/g 11523-0934-02 | Bayer | 1 tube | — | — | FDA listed | — |
| Tinactin 10 mg/g 11523-1190-01 | 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 | — |
| meijer antifungal 10 mg/g 41250-0499-01 | Meijer | 1 tube | — | — | FDA listed | — |
| AVON HeXashield Athletes Foot Cream 10 mg/g 43136-0104-01 | Tai | 1 tube | — | — | FDA listed | — |
| CLARUS Antifungal 1 g/100g 44577-0001-01 | Clinical | 45 g | — | — | FDA listed | — |
| CLARUS Antifungal 10 mg/g 44577-0470-00 | Clinical | 1 tube | — | — | FDA listed | — |
| equate Athletes Foot 10 mg/g 49035-0499-03 | Wal-Mart | 1 tube | — | — | FDA listed | — |
| sunmark antifungal 10 mg/g 50090-3358-00 | A-S | 1 tube | — | — | FDA listed | — |
| CR-371059 Tolnaftate 1% 1 g/100g 50090-6147-00 | A-S | 14.8 g | — | — | FDA listed | — |
| CAREALL Tolnaftate 10 mg/g 51824-0001-01 | New | 28 g | — | — | FDA listed | — |
| Family Wellness Athletes Foot Tolnaftate 1 Cream 10 mg/g 55319-0991-00 | Family | 1 tube | — | — | FDA listed | — |
| Athletes Foot Antifungal .01 mg/10g 55910-0341-24 | Dollar | 1 tube | — | — | FDA listed | — |
| Pedikleer 1 g/100g 57237-0354-15 | Rising | 1 tube | — | — | FDA listed | — |
| Hongo Killer 10 mg/gthis 58593-0286-22 | Efficient | 28 g | — | — | Discontinued | — |
| Family Care Antifungal 10 mg/g 65923-0021-28 | United | 1 tube | — | — | FDA listed | — |
| Winco Antifungal 10 mg/g 67091-0051-28 | WinCo | 1 tube | — | — | FDA listed | — |
| Winco Foods Tolnaftate 10 mg/g 67091-0276-28 | Winco | 1 tube | — | — | FDA listed | — |
| Natureplex Tolnaftate Antifungal 10 mg/g 67234-0032-01 | Natureplex, | 1 tube | — | — | FDA listed | — |
| Tolnaftate Cream 1% 10 mg/g 68016-0152-01 | Pharmacy | 1 tube | — | — | FDA listed | — |
| Tolnaftate 10 mg/g 68071-4245-05 | NuCare | 14.18 g | — | — | FDA listed | — |
| Skinheal Antifungal 1 g/100g 69070-0305-01 | Zhejiang | 1 tube | — | — | FDA listed | — |
| Tolnaftate Cream 1% ANTIFUNGAL 1 g/100g 69396-0016-05 | Trifecta | 1 tube | — | — | FDA listed | — |
| Tolnaftate Cream 1% ANTIFUNGAL 1 g/100g 69396-0042-05 | Trifecta | 1 tube | — | — | FDA listed | — |
| Tolnaftate 1 g/100g 69396-0130-01 | Trifecta | 1 tube | — | — | FDA listed | — |
| Canespies 1 g/100g 69729-0610-05 | OPMX | 1 tube | — | — | FDA listed | — |
| CVS Health Athletes Foot 10 mg/g 69842-0336-14 | CVS | 1 tube | — | — | FDA listed | — |
| Athletes Foot 10 mg/g 70084-0510-01 | Quantum, | 1 tube | — | — | FDA listed | — |
| Aftate Athlete Foot Cream 1 g/100g 70356-0001-01 | Sabel | 28 g | — | — | FDA listed | — |
| TheraCare Antifungal Cream 10 mg/g 71101-0017-01 | Veridian | 1 tube | — | — | FDA listed | — |
| Funginix Af 1 g/100g 71229-0103-11 | The | 28 g | — | — | FDA listed | — |
| Funginix Jock Itch Treatment 1 g/100g 71229-0104-11 | The | 28 g | — | — | FDA listed | — |
| TriTolnacide C 1 g/100mL 73352-0561-10 | Trifluent | 1 bottle | — | — | FDA listed | — |
| Dr.Scholl s Odor X Athlete s Foot 10 mg/g 73469-0618-01 | Scholl's | 1 bottle | — | — | FDA listed | — |
| Thera plus Antifungal Tolnaftate 10 mg/g 80684-0040-01 | FOURSTAR | 1 tube | — | — | FDA listed | — |
| Derman antifungal cream 10 mg/g 81929-0004-01 | Taisho | 1 tube | — | — | FDA listed | — |
| Up and Up Antifungal 10 mg/g 82442-0020-28 | Target | 1 tube | — | — | FDA listed | — |
| Antifungal 1 g/100g 83324-0049-01 | Chain | 1 tube | — | — | FDA listed | — |
| Sylvirene Fungal Nail Renewal 1 g/100mL 85248-0068-01 | Jiangxi | 30 ml | — | — | FDA listed | — |
| Tagrid Athletes Foot Treament 10 mg/g 85384-0008-01 | TAGRID | 100 g | — | — | FDA listed | — |
| Initial Drug Listing - Hermon Athletes Foot 1% Tolnaftate Cream .6 g/60g 85398-0017-01 | Beautivity | 60 g | — | — | FDA listed | — |
| Antifungal Medicated Bar 10 mg/g 85424-0001-01 | RoyceDerm | 232 g | — | — | FDA listed | — |
| Tagrid Antifungal 10 mg/g 85384-0013-01 | TAGRID | 113.4 g | — | — | FDA listed | — |
| Tagrid Antifungal 10 mg/g 85384-0010-01 | TAGRID | 142 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
🏛️
2000
On the market since
Jan 2000
📍
2026
Currently FDA-listed
26 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 Hongo Killer (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 |
|---|---|---|---|
| 58593-0286-01 | 1 TUBE in 1 CARTON (58593-286-01) / 28 g in 1 TUBE | 2000-01-01 | Active |
| 58593-0286-05 | 1 TUBE in 1 CARTON (58593-286-05) / 14 g in 1 TUBE | 2000-01-01 | Active |
| 58593-0286-10 | 1 g in 1 PACKET (58593-286-10) | 2000-01-01 | Active |
| 58593-0286-22 You're viewing this | 28 g in 1 TUBE (58593-286-22) | 2010-01-01 | Discontinued by firm |
Pack size FAQ
What quantity is in NDC 58593-0286-22?
NDC 58593-0286-22 contains 28 g — 28 g in 1 tube.
What is the difference between NDC 58593-0286-22 and NDC 58593-0286-10?
Both are Hongo Killer Tolnaftate 10 mg/g Cream — the drug itself is identical. NDC 58593-0286-22 is the 28 g package, while NDC 58593-0286-10 is the 1 g package.
What NDC number is used to bill for this package of Hongo Killer Tolnaftate 10 mg/g Cream?
Bill NDC 58593-0286-22 — the 11-digit billing format is 58593028622. 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
No longer marketed (per FDA listing data)
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) | — 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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 58593-286-22, 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: 58593-0286-22, written without dashes as 58593028622. 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 58593-0286-22, the first segment (58593) is the labeler code FDA assigned to Efficient Laboratories Inc; the middle segment (0286) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (22) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 3 other package presentations of this same product, including 1 tube (58593-0286-01), 1 tube (58593-0286-05), 1 g (58593-0286-10). 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?
Efficient Laboratories Inc 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 clinically effective in the treatment of most: athlete's foot (tinea pedis) ringworm (tinea corporis) effectively soothes are relieves: itching burning cracking helps prevent most athlete's foot with daily use
⏱️ Dosage and Administration ▾
Directions clean the affected area and dry thoroughly apply a thin layer over the affected area twice daily (morning and night) or as directed by a doctor supervise children in the use of this product for athlete's foot, pay special attention to spaces between the toes. Wear well-fitting, ventilated shoes, and change shoes and socks at least once daily for athlete's foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks. If condition persists, consult a doctor to prevent athlete's foot, wash the feet, and dry thoroughly.
Apply a thin layer over the affected area twice daily (morning and/or night) this product is not effective on scalp or nails
⚠️ Warnings ▾
Warnings For external use only. Do not use on children under 2 years of age unless directed by a doctor For Diaper Rash When using this product When using this product avoid contact with eyes Stop use and ask a doctor if irritation occurs there is no improvement within 4 weeks Keep out of reach of children. If swallowed, get medical help or, contact a Poison Control Center right away: 800-222-1222.
📦 Storage and Handling ▾
Other information store at 15°to 30°C (59°to 86°F) Tamper Evident: DO NOT USE IF SEAL ON TUBE IS BROKEN OR MISSING.
🧪 Active Ingredient ▾
Active ingredient Tolnaftate 1%
🧪 Inactive Ingredients ▾
Inactive ingredients ceteth-20, cetyl alcohol, chlorocresol, mineral oil, monobasic sodium phosphate, petrolatum, propylene glycol, purified water, stearyl alcohol
🎯 Purpose ▾
Purpose Antifungal
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.