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Fungi Nail Toe and Foot Tolnaftate 1 g/100g Ointment — NDC 55505-185-50 (Billing 55505-0185-50)

by Kramer Laboratories · 1 TUBE in 1 CARTON / 20 g in 1 TUBE

This is a package of Fungi Nail Toe and Foot Tolnaftate 1 g/100g Ointment from Kramer Laboratories, marketed since Nov 2018 and currently FDA-listed. It is this product's only package size.

NDC 55505-0185-50
🏷️ FDA NDC (as labeled) 55505-185-50 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 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

NDC database record

One package, one record: these facts belong to NDC 55505-185-50 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
55505 labeler · 185 product · 50 package
Package marketed since
Jun 1, 2019
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 5550518550 0
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 55505-185-50
Product NDC 55505-185
11-digit billing NDC 55505018550
RxCUI 199126
UNII 06KB629TKV
Application # M005
SPL Set ID e21ccb83-54ff-4605-80bf-7b4b789c7cb7
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2018-11-15
Route TOPICAL
Dosage form OINTMENT
Substance TOLNAFTATE
Quick answers
  • RxCUI (RxNorm): 199126
Why two NDCs? The FDA registers this code as 55505-185-50 — 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 → 55505-0185-50. 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.

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 gPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
55505-0185-50 You're viewing this Main listing 1 TUBE in 1 CARTON / 20 g in 1 TUBE 2019-06-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Tolnaftate Cream 1% ANTIFUNGAL 1 g/100g 70000-0084-01 CARDINAL 1 tube $0.119 — Availability likely —
Tolnaftate Antifungal 1 g/100g 51672-2020-01 Sun 1 tube $0.150 — Availability likely —
Tolnaftate Antifungal 1 g/100g 70677-1001-01 STRATEGIC 1 tube $0.150 — Availability likely —
Hi Vetic 1 g/100g 49873-0056-01 Sato 1 tube — — FDA listed —
Fungi Nail Toe and Foot 1 g/100gthis 55505-0185-50 Kramer 1 tube — — FDA listed —
Phytozine Ringworm Treatment Maximum Strength 1 g/100g 71229-0101-11 The 28 g — — FDA listed —
Healmusz Fungal Nail 1 g/100g 85248-0056-01 Jiangxi 30 g — — FDA listed —
Dryello Dual Action Relief for Athlete Foot 1 g/100g 85565-0002-01 ProPedix, 2 applicators — — FDA listed —
Dryello Tolnaftate 1% Antifungal 1 g/100g 85565-0005-01 ProPedix, 2 applicators — — FDA listed —
Aftate Athlete Foot Cream 1 g/100g 70356-0001-01 Sabel 28 g — — FDA listed —
CLARUS Antifungal 1 g/100g 44577-0001-01 Clinical 45 g — — FDA listed —
Antifungal Medicated Body Wash 1 g/100g 83004-0012-01 Rida 56 g — — FDA listed —
Inlifay ANTIFUNGAL 1 g/100g 83566-0609-01 Guangdong 232 g — — FDA listed —
Odor-Eaters Athletes Foot 1 g/100g 10157-3100-01 Blistex 1 tube — — FDA listed —
Rapid MicroGel 1 g/100g 49406-0005-28 The 28 g — — FDA listed —
Terramed Just Think Comfort Armor Antifungal Medicated 1 g/100g 83004-0017-01 Rida 120 g — — FDA listed —
Tolnaftate Cream 1% ANTIFUNGAL 1 g/100g 69396-0016-05 Trifecta 1 tube — — FDA listed —
Canespies 1 g/100g 69729-0610-05 OPMX 1 tube — — FDA listed —
Terramed Just Think Comfort Armor Antifungal Body Wash Tea Tree 1 g/100g 83004-0032-01 Rida 56 g — — FDA listed —
Skinheal Antifungal 1 g/100g 69070-0305-01 Zhejiang 1 tube — — FDA listed —
Funginix Jock Itch Treatment 1 g/100g 71229-0104-11 The 28 g — — FDA listed —
Kdman 1 g/100g 87723-6625-01 Dongguan 200 g — — FDA listed —
Funginix Af 1 g/100g 71229-0103-11 The 28 g — — FDA listed —
Quali Life ANTIFUNGAL PERSIMMON 1 g/100g 83566-0606-01 Guangdong 300 g — — FDA listed —
Quali Life ANTIFUNGAL TEA TREE 1 g/100g 83566-0611-01 Guangdong 300 g — — FDA listed —
Athlete Foot Medicated bar 1 g/100g 85398-0007-01 Beautivity 232 g — — FDA listed —
Pedikleer 1 g/100g 57237-0354-15 Rising 1 tube — — FDA listed —
Hermon Antifungal Bar 1 g/100g 85261-0601-01 Haikou 232 g — — FDA listed —
Defense Antifungal Medicated Bar 1 g/100g 70856-3581-02 Defense 1 not — — FDA listed —
Quali Life ANTIFUNGAL CHARCOAL 1 g/100g 83566-0607-01 Guangdong 300 g — — FDA listed —
Kerasal for Athletes Foot Silky Clear 1 g/100g 16864-0100-01 Advantice 1 tube — — Discontinued —
Inlifay ANTIFUNGAL 1 g/100g 60771-0040-01 Guangzhou 232 g — — FDA listed —
Tea Tree Oil Antifungal 1 g/100g 85593-0105-01 Guangzhou 100 g — — FDA listed —
Activ-Charcoal Antifungal 1 g/100g 87800-0002-01 HONG 100 g — — FDA listed —
OAKDOLCHE Tea Tree Oil Antifungal 1 g/100g 87864-0001-01 Nanjing 400 g — — FDA listed —
Dryello Tolnaftate 1% Antifungal 1 g/100g 85565-0008-01 ProPedix, 2 applicators — — FDA listed —
VXGXO antifungal with tea tree oil 1 g/100g 83566-0620-01 Guangdong 200 g — — FDA listed —
BlissCare tea tree oil antifungal 1 g/100g 83566-0619-01 Guangdong 115 g — — FDA listed —
Tolnaftate 1% Antifungal Soaps 1 g/100g 85158-0002-01 Shenzhen 2 pouches — — 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

🏛️
2018
On the market since
Nov 2018
📍
2026
Currently FDA-listed
8 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.

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.

Manufacturer & labeler

LabelerKramer Laboratories
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code55505
First marketedNov 2018
Product typeHuman Otc Drug
Portfolio26 products on file

More NDCs from Kramer Laboratories labeler code 55505

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 📦 Storage and Handling 🧪 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 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 32 words ▾

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 98 words ▾

Directions Clean affected area with soap and warm water and dry thoroughly. Apply a thin layer of Fungi-Nail® Anti-Fungal Ointment 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).

This product is not effective on the scalp or nails. Supervise children in the use of this product.

⚠️ Warnings 5 words ▾

Warnings For external use only.

📦 Storage and Handling 30 words ▾

Other information Store at room temperature 15º – 30º C (59º – 86º F) Protect from freezing. If freezing occurs warm to room temperature. Keep carton for full product information.

🧪 Active Ingredient 6 words ▾

Active Ingredient Purpose Tolnaftate 1% Anti-fungal

🧪 Inactive Ingredients 71 words ▾

Inactive ingredients 3-O-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 6 words ▾

Active Ingredient Purpose Tolnaftate 1% Anti-fungal

📄 Do Not Use 15 words ▾

Do not use on children under 2 years of age unless directed by a doctor.

📄 When Using This Product 8 words ▾

When using this product avoid contact with eyes.

📄 Stop Use and Ask a Doctor If 16 words ▾

Stop use and ask a doctor if Irritation occurs. There is no improvement within 4 weeks.

📄 Keep Out of Reach of Children 30 words ▾

KEEP THIS AND ALL MEDICATION OUT OF THE REACH OF CHILDREN. In case of accidental ingestion, contact a physician, emergency medical care facility or Poison Control Center immediately for advice.

📄 Questions or Comments 2 words ▾

Questions? 1-800-824-4894

📄 Package Label / Principal Display Panel 160 words ▾

PRINCIPAL DISPLAY PANEL MAXIMUM STRENGTH FUNGI-NAIL ® ANTI-FUNGAL OINTMENT with brush applicator CLINICALLY PROVEN TO CURE AND PREVENT FUNGAL INFECTIONS TRIPLE ACTION FORMULA ✓ Kills Fungus ✓ Stops Itching & Burning ✓ Restores Skin Health + Cures Most Athlete's Foot CLINICALLY PROVEN INGREDIENT PLUS Aloe & Tea Tree Oil NET WT

0.7OZ (20 g) Not actual size. New Formula FUNGI-NAIL ® Maximum Strength Anti-Fungal plus 9 natural oils: ○ aloe vera ○ tea tree ○ coconut ○ lavender ○ olive ○ thyme ○ cloves ○ cinnamon ○ eucalyptol and antioxidant Vitamin E For more information about Fungi-Nail ® and money back guarantee, visit us at funginail.com Fungi-Nail® is Specially Formulated to Kill Fungus and Restore Skin Health Deep Penetrating Medicine that Stays in Place Convenient & Easy to Apply Kramer Laboratories, Inc., Bridgewater, NJ 08807 1-800-824-4894 For best results treat skin around all toenails and in between toes.

Not for nail or scalp fungus. Cures most athlete’s foot. K0126

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 — 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 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 Kramer Laboratories. Listing status can change — the directory data on this page refreshes weekly.
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.
← 55505-0177-26 · Kramer 55505-0193-51 · Kramer →
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.