HomeNDC LookupIngredientsTolnaftate › 69729-0610-05
CANESPIES TOLNAFTATE 1 g/100g Cream — NDC 69729-0610-05 package photo

CANESPIES TOLNAFTATE 1 g/100g Cream

by OPMX LLC · 1 TUBE in 1 BOX (69729-610-05) / 14 g in 1 TUBE (69729-610-01)
NDC 69729-0610-05
🏷️ FDA NDC (as labeled) 69729-610-05 billing pads the product 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 →

🆔 Identity & classification

FDA NDC (as labeled) 69729-610-05
Product NDC 69729-610
11-digit billing NDC 69729061005
RxCUI 103951
UNII 06KB629TKV
UPC 0856828008205
Application # M005
SPL Set ID e2f9eedc-3c43-416b-85b5-ba07fb5fb4db
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-07-26
Route TOPICAL
Dosage form CREAM
Substance TOLNAFTATE
Why two NDCs? The FDA registers this code as 69729-610-05 — 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 → 69729-0610-05. 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

LabelerOPMX LLC
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code69729
First marketedJul 2022
Product typeHuman Otc Drug
Portfolio87 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 I835H2IHHX
    A waxy substance derived from plant oils, used as an emulsifier and solubilizer to help mix oil and water ingredients together and keep them blended throughout the product's shelf life.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII 36W53O7109
    Chlorocresol is a phenolic antimicrobial chemical used as a preservative in liquid medicines and injectable solutions. It prevents bacterial and fungal growth to maintain product safety and shelf-life.
  • UNII T5L8T28FGP
    Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
  • UNII I9O0E3H2ZE
    Paraffin is a waxy, petroleum-derived substance used as a coating, lubricant, and hardening agent in tablets and capsules. It helps protect the medicine from moisture and gives pills a smooth finish.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII 3980JIH2SW
    A salt form of phosphoric acid that acts as a buffer and pH adjuster in medicines. It helps keep the product at the correct acidity level for stability and effectiveness.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

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

The official label also statesCETETH-20, CETYL ALCOHOL, CHLOROCRESOL, MINERAL OIL, PROPYLENE GLYCOL, SODIUM PHOSPHATE MONOBASIC, WHITE SOFT PARAFFIN, PURIFIED WATER

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 DailyMedingredient 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 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
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/g 58593-0286-01 Efficient 1 tube FDA listed
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/100gthis 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
Hi Vetic 1 g/100g 49873-0056-01 Sato 1 tube 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
Phytozine Ringworm Treatment Maximum Strength 1 g/100g 71229-0101-11 The 28 g 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
Terramed Just Think Comfort Armor Antifungal Body Wash Tea Tree 1 g/100g 83004-0032-01 Rida 56 g FDA listed
Dryello Dual Action Relief for Athlete Foot 1 g/100g 85565-0002-01 ProPedix, 2 applicators FDA listed
Kdman 1 g/100g 87723-6625-01 Dongguan 200 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
Hermon Antifungal Bar 1 g/100g 85261-0601-01 Haikou 232 g FDA listed
Dryello Tolnaftate 1% Antifungal 1 g/100g 85565-0005-01 ProPedix, 2 applicators FDA listed
Fungi Nail Toe and Foot 1 g/100g 55505-0185-50 Kramer 1 tube 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

🏛️
2022
On the market since
Jul 2022
📍
2026
Currently FDA-listed
4 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
69729-0610-05 You're viewing this 1 TUBE in 1 BOX (69729-610-05) / 14 g in 1 TUBE (69729-610-01) 2022-07-26 Active

🧭 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 FDA registers it as 69729-610-05, 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: 69729-0610-05, written without dashes as 69729061005. 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 69729-0610-05, the first segment (69729) is the labeler code FDA assigned to OPMX LLC; the middle segment (0610) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (05) identifies this exact package size and type. Together they name one specific package of one specific product.
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 OPMX LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
OPMX 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 44 words

USES PROVEN CLINICALLY EFFECTIVE IN THE TREATMENT OF ATHLETE'S FOOT (TINEA PEDIS), JOCK ITCH (TINEA CRURIS), RINGWORM (TINEA CORPORIS) PROVEN EFFECTIVE IN THE PREVENTION OF ATHLETE'S FOOT EFFECTIVELY SOOTHES AND RELIEVES ITCHING ASSOCIATED WITH JOCK ITCH, SCALY SKIN BETWEEN THE TOES AND BURNING FEET

⏱️ Dosage and Administration 92 words

DIRECTIONS WASH AFFECTED AREA AND DRY THOROUGHLY APPLY A THIN LAYER 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, VENTILLATED 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 WEKS. IF CONDITION PERSISTS LONGER CONSULT A DOCTOR THIS PRODUCT IS NOT EFFECTIVE ON THE SCALP OR NAILS

⚠️ Warnings 40 words

WARNINGS For external use only. STOP USE AND ASK A DOCTOR IF IRRITATION OCCURS THERE IS NO IMPROVEMENT WITHIN 4 WEEKS. DO NOT USE ON CHILDREN UNDER 2 YEARS OF AGE EXCEPT UNDER THE ADVICE AND SUPERVISION OF A DOCTOR.

🧪 Active Ingredient 4 words

ACTIVE INGREDIENTS TOLNAFTATE 1%

🧪 Inactive Ingredients 18 words

INACTIVE INGREDIENTS CETETH-20, CETYL ALCOHOL, CHLOROCRESOL, MINERAL OIL, PROPYLENE GLYCOL, SODIUM PHOSPHATE MONOBASIC, WHITE SOFT PARAFFIN, PURIFIED WATER

🎯 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 ↗
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.