Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Tolnaftate Antifungal Liquid Spray 1.5 g/150g Aerosol, Spray, 150 g — NDC 69842-185-53 (Billing 69842-0185-53)
by CVS Pharmacy · 150 g in 1 CANISTER
This is a package of 150 g of Tolnaftate Antifungal Liquid Spray 1.5 g/150g Aerosol, Spray from CVS Pharmacy, marketed since Jul 2018 and currently FDA-listed. It is this product's only package size.
NDC 69842-0185-53
🏷️ FDA NDC (as labeled)
69842-185-53
billing pads the product segment with a zero
🗂️ 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 →
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
69842-185-53
Product NDC
69842-185
11-digit billing NDC
69842018553
RxCUI
313421
UNII
06KB629TKV
Application #
M005
SPL Set ID
96cc594d-85c8-4f62-bc0a-3176c8739f21
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2018-07-31
Route
TOPICAL
Dosage form
AEROSOL, SPRAY
Substance
TOLNAFTATE
Quick answers
- RxCUI (RxNorm): 313421
Why two NDCs?
The FDA registers this code as 69842-185-53 — 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 → 69842-0185-53. 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
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.
- RxClass (NLM) · catalog refreshed Oct 1, 2026
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 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.
Patient education
Supplement & herbal interactions
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.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about Antifungal Liquid Spray?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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.
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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 2, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 69842-0185-53 You're viewing this Main listing | 150 g in 1 CANISTER | 2018-07-31 | — | Active |
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price 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/150gthis 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/100mL 85384-0017-01 | TAGRID | 100 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2018
On the market since
Jul 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.
- FDA Orange Book · refreshed Sep 3, 2026
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 3K9958V90M
A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
-
UNII 1P9D0Z171K
BHT is a synthetic antioxidant that prevents fats and oils in medicines from breaking down and becoming rancid. It helps keep the product stable and effective during storage.
-
UNII BXR49TP611
Isobutane is a liquefied gas used as a propellant in aerosol inhalers and sprays. It helps push the medicine out of the container so you can breathe or spray it as directed.
-
UNII 58CG7042J1
A synthetic liquid polymer made from propylene glycol and fatty alcohol components. It functions as an emulsifier and solubilizer, helping mix oil and water-based ingredients and keep them blended throughout the product's shelf life.
4 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesBHT, isobutane, PPG-12-buteth-16, SD alcohol 40-B
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.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
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
LabelerCVS Pharmacy
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code69842
First marketedJul 2018
Product typeHuman Otc Drug
Portfolio550 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 openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
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
📄 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 ▾
Uses proven clinically effective in the treatment of athlete's foot (tinea pedis) and ringworm (tinea corporis) prevent recurrence of most athlete's foot with daily use for effective relief of itching, cracking and burning
⏱️ Dosage and Administration ▾
Directions wash affected area and dry thoroughly shake can well and spray a thin layer of the product over 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 if condition persists, consult a doctor to prevent athlete's foot: wash the feet and dry thoroughly; spray a thin layer of the product to the feet once or twice daily (morning and/or night) this product is not effective on the scalp or nails if nozzle clogs, clean with a pin
⚠️ Warnings ▾
Warnings For external use only. Flammable: Contents under pressure. Avoid spraying in eyes. Do not use or store near heat or open flame.
Do not puncture or incinerate container. Do not store at temperature above 120°F. Keep out of reach of children.
Use only as directed.Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal. When using this product avoid contact with the eyes or mouth use only as directed Stop use and ask a doctor if irritation occurs no improvement within 4 weeks for athlete's foot and ringworm Do not use on children under 2 years of age unless directed by a doctor. Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Do not use on children under 2 years of age unless directed by a doctor.
🧪 Active Ingredient ▾
Active ingredient Tolnaftate 1%
🧪 Inactive Ingredients ▾
Inactive ingredients BHT, isobutane, PPG-12-buteth-16, SD alcohol 40-B
🎯 Purpose ▾
Purpose Antifungal
📄 When Using This Product ▾
When using this product avoid contact with the eyes or mouth use only as directed
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if irritation occurs no improvement within 4 weeks for athlete's foot and ringworm
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
📄 Other Information ▾
Other information store between 20º and 30ºC (68º and 86ºF)
📄 Questions or Comments ▾
Questions? call 1-866-964-0939
📄 Package Label / Principal Display Panel ▾
Principal Display Panel CVS Health Antifungal Athlete's Foot Liquid Spray ANTIFUNGAL / TOLNAFTATE 1% Cures most athlete's foot & prevents recurrences Relieves itching, cracking & burning NET WT
5.3 OZ (150g) carton
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 ↗
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 CVS Pharmacy. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
CVS Pharmacy 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.
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.