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Kerasal Athletes Foot powder Tolnaftate 1 g/100g Spray, 57 g — NDC 16864-0110-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Kerasal Athletes Foot powder Tolnaftate 1 g/100g Spray, 57 g — NDC 16864-110-01 (Billing 16864-0110-01)

by Advantice Health, LLC · 57 g in 1 CAN

This is a package of 57 g of Kerasal Athletes Foot powder Tolnaftate 1 g/100g Spray from Advantice Health, LLC, no longer marketed (first marketed Feb 2022), no longer in the FDA NDC Directory. It is this product's only package size.

NDC 16864-0110-01
🏷️ FDA NDC (as labeled) 16864-110-01 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ 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

⚠️
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 Sep 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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 16864-110-01
Product NDC 16864-110
11-digit billing NDC 16864011001
RxCUI 705934
UNII 06KB629TKV
Application # M005
SPL Set ID 470d8424-21b8-48e5-8f33-e8baf65c2fb0
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Sep 2026)
Marketing start 2022-02-28
Marketing end 2026-09-30
Route TOPICAL
Dosage form SPRAY
Substance TOLNAFTATE
Quick answers
  • RxCUI (RxNorm): 705934
Why two NDCs? The FDA registers this code as 16864-110-01 — 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 → 16864-0110-01. 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.

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.
📖 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 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
16864-0110-01 You're viewing this Main listing 57 g in 1 CAN 2022-02-28 — Active

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/100gthis 16864-0110-01 Advantice 57 g — — Discontinued —
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/g 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 —
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
Feb 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.

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 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • 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 ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • 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 C04977SRJ5
    Ceramide NG is a naturally occurring lipid compound that helps form protective barriers in skin and cosmetic formulations. It functions as an emollient and skin-conditioning agent, helping products retain moisture and maintain smooth texture.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII 2R04ONI662
    Eucalyptus oil is a fragrant liquid extracted from eucalyptus tree leaves. It's used in medicines as a flavor, scent, or soothing agent in topical products and cough preparations.
  • 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 A8289P68Y2
    Isododecane is a lightweight liquid hydrocarbon used as a solvent and spreadability agent in topical formulations. It helps dissolve active ingredients and makes the product easier to apply and absorb into the skin.
  • UNII AV092KU4JH
    A natural oil extracted from peppermint plants. It's used as a flavoring agent to mask bitter tastes and add a refreshing mint flavor to medicines, making them easier to take.
  • UNII 24SC3U704I
    A powdery carbohydrate extracted from tapioca plant roots. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your digestive system.
  • UNII VIF565UC2G
    Tea tree oil is an essential oil extracted from the leaves of the Australian tea tree plant. In medicines, it typically serves as a flavoring agent, fragrance, or antimicrobial component in topical formulations.

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

The official label also statesalcohol, aloe vera leaf, alpha-tocopherol acetate, butylated hydroxytoluene, ceramide NG, dimethicone, eucalyptus oil, isobutane, isododecane, methylal, peppermint oil, tapioca starch, tea tree oil

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.

Manufacturer & labeler

LabelerAdvantice Health, LLC
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code16864
First marketedFeb 2022
Product typeHuman Otc Drug
Portfolio11 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 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
🎯 Indications and Usage 31 words ▾

Uses Proven clinically effective in the treatment of most athlete's foot (tinea pedis) Helps prevent most athlete's foot with daily use For effective relief of itching, cracking, burning, scaling and discomfort

⏱️ Dosage and Administration 93 words ▾

Directions Wash the 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 pay special attention to spaces between the toes; wear well-fitting, ventilated shoes and change shoes and socks at least once daily Use daily for 4 weeks; if condition persists longer, ask a doctor To prevent athlete's foot, apply once or twice daily (morning and/or night, or as directed by a doctor) This product is not effective on the scalp or nails.

⚠️ Warnings 108 words ▾

Warnings For external use only Extremely 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 the contents can be harmful or fatal. Do not puncture or incinerate. Contents under pressure.

Do not store at temperatures above 120°F Stop use and ask 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.

📦 Storage and Handling 6 words ▾

Other information Store between 20-25°C (68-77°F)

🧪 Active Ingredient 6 words ▾

Active ingredient (To Deliver) Tolnaftate 1%

🧪 Inactive Ingredients 25 words ▾

Inactive ingredients alcohol, aloe vera leaf, alpha-tocopherol acetate, butylated hydroxytoluene, ceramide NG, dimethicone, eucalyptus oil, isobutane, isododecane, methylal, peppermint oil, tapioca starch, tea tree oil

🎯 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 ↗

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 ✓ 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.
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 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.
Who lists this product with the FDA?
Advantice Health, 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.
← 16864-0100-01 · Advantice 16864-0140-01 · Advantice →
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.