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Walgreens Medicated Antifungal Athletes Foot TOLNAFTATE 10 mg/g Spray, 130 g

by Formulated Solutions, LLC · 130 g in 1 CAN (23667-818-01)
NDC 23667-0818-01
🏷️ FDA NDC (as labeled) 23667-818-01 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ Data synced Jul 14, 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

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Mar 2026. 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) 23667-818-01
Product NDC 23667-818
11-digit billing NDC 23667081801
RxCUI 705934
UNII 06KB629TKV
UPC 0311917048659
Application # M005
SPL Set ID 46c63c9a-d484-382e-e054-00144ff8d46c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Mar 2026)
Marketing start 2017-01-23
Route TOPICAL
Dosage form SPRAY
Substance TOLNAFTATE
Why two NDCs? The FDA registers this code as 23667-818-01 — 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 → 23667-0818-01. 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

LabelerFormulated Solutions, LLC
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code23667
First marketedJan 2017
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...
📖 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.

🧪 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.

We could not link this NDC to a current FDA Structured Product Label. An inactive-ingredient list is therefore not available from this source.
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 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.
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

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Tolnafate 1.3 g/130g 70000-0322-01 LEADER/ 130 g $0.033 — Availability likely —
Tolnaftate 1.3 g/113g 00363-0216-13 Walgreen 113 g — — FDA listed —
Tolnaftate 1.3 g/130g 00363-1746-00 Walgreens 130 g — — FDA listed —
Blistex Odor-Eaters Powder 1 g/100g 10157-4645-01 Blistex 113 g — — FDA listed —
Lotrimin Daily Prevention Deo 10 mg/g 11523-0010-01 Bayer 160 g — — FDA listed —
Lotrimin Daily Prevent Deodorant 10 mg/g 11523-0136-01 Bayer 160 g — — FDA listed —
Tinactin Deodorant 10 mg/g 11523-0137-01 Bayer 133 g — — FDA listed —
Tinactin Jock Itch 10 mg/g 11523-0138-01 Bayer 133 g — — FDA listed —
Tinactin 10 mg/g 11523-0139-01 Bayer 133 g — — FDA listed —
Tinactin Antifungal 10 mg/g 11523-4162-01 Bayer 133 g — — FDA listed —
Tolnaftate 1.3 g/130g 11822-0782-04 Rite 130 g — — FDA listed —
Kerasal Athletes Foot powder 1 g/100g 16864-0110-01 Advantice 57 g — — FDA listed —
Tolnafate 1.3 g/130g 21130-0215-00 Better 130 g — — FDA listed —
GoodSense Powder Jock Itch Antifungal 10 mg/g 23667-0806-01 Formulated 130 g — — Discontinued —
Walgreens Maximum Strength Jock Itch Antifungal 10 mg/g 23667-0807-01 Formulated 130 g — — Discontinued —
Meijer Maximum Strength Jock Itch Relief Antifungal 10 mg/g 23667-0809-01 Formulated 130 g — — Discontinued —
Meijer Maximum Strength Anthletes foot Antifungal 10 mg/g 23667-0810-01 Formulated 130 g — — Discontinued —
Signature Athletes Foot Antifungal 10 mg/g 23667-0814-01 Formulated 130 g — — Discontinued —
Walgreens Medicated Antifungal Athletes Foot 10 mg/gthis 23667-0818-01 Formulated 130 g — — Discontinued —
Tolnaftate 1.3 g/130g 30142-0841-01 Kroger 130 g — — FDA listed —
Tolnaftate 1.13 g/113g 36800-0023-04 Topco 113 g — — FDA listed —
Tolnafate 1.3 g/130g 36800-0876-46 Topco 130 g — — FDA listed —
Tolnaftate 1.3 g/130g 36800-0877-46 Topco 130 g — — FDA listed —
Tolnaftate 1.13 g/113g 37808-0514-40 HEB 113 g — — FDA listed —
Tolnafate 1.3 g/130g 37808-0530-46 HEB 130 g — — FDA listed —
Tolnaftate 1.3 g/130g 41250-0563-46 Meijer 130 g — — Discontinued —
Tolnaftate 1.13 g/113g 41520-0086-04 Foodhold 113 g — — FDA listed —
Derman Antifungal 10 mg/g 54312-0230-01 Compania 130 g — — FDA listed —
Antifungal Powder 10 mg/g 55301-0874-01 ARMY 130 g — — FDA listed —
Fungi Nail Everyday Antifungal Powder 1.3 g/130g 55505-0234-81 Kramer 130 g — — FDA listed —
Hongo Killer .1 g/10g 58593-0285-04 Efficient 130 g — — FDA listed —
Tolnafate 1.3 g/130g 63868-0181-46 Chain 130 g — — FDA listed —
Tolnafate 1.3 g/130g 63941-0540-46 VALU 130 g — — FDA listed —
Tolnafate 1.3 g/130g 63941-0541-46 VALU 130 g — — FDA listed —
Tolnafate 1.3 g/130g 68016-0653-46 Chain 130 g — — FDA listed —
Tolnafate 1.3 g/130g 68016-0663-46 Chain 130 g — — FDA listed —
Tolnafate 1.3 g/130g 69842-0512-46 CVS 130 g — — FDA listed —
Tolnafate 10 mg/g 79481-0607-01 Meijer 130 g — — FDA listed —
Foot Odor Control Powder 10 mg/g 79481-0622-01 Meijer 113 g — — FDA listed —
Tolnafate 10 mg/g 79481-0623-01 Meijer 130 g — — FDA listed —
Tolnafate 1.3 g/130g 79903-0016-46 Wal-Mart 130 g — — FDA listed —
Derman Antifungal Powder Tolnaftate 10 mg/g 81929-0001-01 Taisho 1 can — — FDA listed —
Tolnaftate 10 mg/g 82442-0402-01 Target 113 g — — FDA listed —
Tolnafate 10 mg/g 83324-0234-46 Chain 130 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 —
Dr. Scholls Instant Cool Athletes foot treatment with Menthol 10 mg/g 73469-0691-01 Scholl's 150 g — — 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

🏛️
2017
On the market since
Jan 2017
📍
2026
Currently FDA-listed
9 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
23667-0818-01 You're viewing this 130 g in 1 CAN (23667-818-01) 2017-01-23 Discontinued by firm

🧭 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 — 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.
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 23667-818-01, 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: 23667-0818-01, written without dashes as 23667081801. 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 23667-0818-01, the first segment (23667) is the labeler code FDA assigned to Formulated Solutions, LLC; the middle segment (0818) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
Who lists this product with the FDA?
Formulated Solutions, 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 🎯 Purpose
🎯 Indications and Usage 32 words ▾

Uses proven clinically effective in the treatment of most athlet's foot (tinea pedis) and ringworm (tinea corporis) helps prevent most athlete's foot with daily use for effective relief if itching, burning, cracking

⏱️ Dosage and Administration 97 words ▾

Directions wash affected area and dry thoroughly shake can well and spray a thin layer over affected area twice daily (morning and night) supervise children in the use of this product for athlete's foot: pay special attention to spaces between the toas, wear well-fitting, ventilated shoes and change shoes and sucks at least once daily use daily for 4 weeks; if condition persist longer, ask a doctor to prevent athlete's foot, apply once or twice daily (morning and/or night) this product is not effective on the scalp or nails In case of clogging, clean nozzle with pin

⚠️ Warnings 109 words ▾

Warnings For external use only Flammable: Do not use while smoking or near heat or flame Do not use on children under 2 years of age unless directed by a doctor When using this product avoid contact with the eyes use only as directed intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal contents under pressure. Do not punture or incinerate. Do not store at temperature above 120°F (49°C).

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 (1-800-222-1222).

🧪 Active Ingredient 6 words ▾

Active ingredient Tolnaftate 1% Purpose Antifungal

🧪 Inactive Ingredients 17 words ▾

Inactive Ingredients alcohol denat, aluminum starch octenylsuccinate, isobutane, isopropyl myristate, propylene carbonate, sorbitan monooleate, stearalkonium hectorite, talc

🎯 Purpose 2 words ▾

Purpose Antifungal

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 23667-0817-01 · Formulated 23667-0819-01 · Formulated →
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.