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Athletes Foot Tolnaftate 10 mg/g Aerosol, Spray, 130 g — NDC 00536-1481-01 package photo

Athletes Foot Tolnaftate 10 mg/g Aerosol, Spray, 130 g

by Rugby Laboratories · 130 g in 1 CAN (0536-1481-01)
NDC 00536-1481-01
🏷️ FDA NDC (as labeled) 0536-1481-01 billing pads the labeler segment with a zero
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 →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 0536-1481-01
Product NDC 0536-1481
11-digit billing NDC 00536148101
NCPDP billing unit GM — per gram (weight)
RxCUI 705934
UNII 06KB629TKV
UPC 0305361481018
Application # M005
SPL Set ID 50c46cf5-3e64-9e0f-e063-6294a90a2317
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-05-01
Route TOPICAL
Dosage form AEROSOL, SPRAY
Substance TOLNAFTATE
Why two NDCs? The FDA registers this code as 0536-1481-01 — a 4-4-2 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 labeler segment → 00536-1481-01. 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

LabelerRugby Laboratories
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code00536
First marketedMay 2026
Product typeHuman Otc Drug
Portfolio149 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...
📖 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.

💡 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 24H4NWX5CO
    Kaolin is a naturally occurring clay mineral. It's used in tablets and capsules as a filler and absorbent to add bulk, improve texture, and help bind ingredients together.
  • 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.
  • UNII 1G5HNE09V8
    A plant-based ingredient derived from whole corn. It serves as a filler and binder to add bulk and help hold the tablet or capsule together during manufacturing.

6 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesISOBUTANE, SD ALCOHOL 40-B, KAOLIN, ZEA MAYS (CORN) STARCH, BHT, PPG-12-BUTETH-16

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.

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 gPer package
Retail pharmacies payNADAC · weekly $0.033 $4.28 / 130 g
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.
NADAC price history (per g) — tap or hover for the price & month
Aug 2026 $0.033 $0.033
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
Athletes Foot 10 mg/gthis 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/150g 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 —
Tinactin Antifungal 10 mg/g 11523-4162-01 Bayer 133 g — — FDA listed —
Lotrimin Daily Prevention Deo 10 mg/g 11523-0010-01 Bayer 160 g — — FDA listed —
Tinactin Jock Itch 10 mg/g 11523-0138-01 Bayer 133 g — — FDA listed —
Derman Antifungal 10 mg/g 54312-0230-01 Compania 130 g — — FDA listed —
Lotrimin Daily Prevent Deodorant 10 mg/g 11523-0136-01 Bayer 160 g — — FDA listed —
Foot Odor Control Powder 10 mg/g 79481-0622-01 Meijer 113 g — — FDA listed —
Antifungal Powder 10 mg/g 55301-0874-01 ARMY 130 g — — FDA listed —
Tinactin 10 mg/g 11523-0139-01 Bayer 133 g — — FDA listed —
Derman Antifungal Powder Tolnaftate 10 mg/g 81929-0001-01 Taisho 1 can — — FDA listed —
Tinactin Deodorant 10 mg/g 11523-0137-01 Bayer 133 g — — FDA listed —
Antifungal Liquid 10 mg/g 46122-0839-35 AmerisourceBergen 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

🏛️
2026
On the market since
May 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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
00536-1481-01 You're viewing this 130 g in 1 CAN (0536-1481-01) 2026-05-01 Active

📄 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 33 words ▾

Uses cures most athlete's foot (tinea pedis), ringworm (tinea corporis) and jock itch (tinea cruris) helps prevent most athlete's foot with daily use relieves itching, burning, cracking, and chafing associated with jock itch

⏱️ Dosage and Administration 123 words ▾

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 to prevent athlete's foot, shake can well and spray a thin layer of the product to the feet once or twice daily (morning and/or night) 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 this product is not effective on the scalp or nails

⚠️ Warnings 117 words ▾

Warnings For external use only. Extremely Flammable: Keep away from fire, sparks, and heated surfaces. Contents under pressure.

Do not puncture or incinerate. Do not store at temperature above 120°F. Do not use on children under 2 years of age unless directed by a doctor.

When using this product avoid spraying in eyes use only as directed intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal Stop use and ask a doctor if there is no improvement within 4 weeks for athlete's foot and ringworm; 2 weeks for jock itch irritation occurs Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

🧪 Active Ingredient 4 words ▾

Active ingredient Tolnaftate 1%

🧪 Inactive Ingredients 13 words ▾

Inactive ingredients ISOBUTANE, SD ALCOHOL 40-B, KAOLIN, ZEA MAYS (CORN) STARCH, BHT, PPG-12-BUTETH-16

🎯 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 ↗
← 00536-1480-34 · Rugby 00536-1483-59 · Rugby →
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.