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Athletes Foot BUTENAFINE HYDROCHLORIDE 10 mg/g Cream — NDC 70677-1269-1 (Billing 70677-1269-01)

by STRATEGIC SOURCING SERVICES LLC · 1 TUBE in 1 CARTON / 30 g in 1 TUBE

This is a package of Athletes Foot BUTENAFINE HYDROCHLORIDE 10 mg/g Cream from STRATEGIC SOURCING SERVICES LLC, marketed since Nov 2024 and currently FDA-listed; retail pharmacies pay about $0.3070 per g (NADAC). It is this product's only package size.

NDC 70677-1269-01
🏷️ FDA NDC (as labeled) 70677-1269-1 billing pads the package segment with a zero
OTC Generic On market Non-controlled ⇄ 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 70677-1269-1
Product NDC 70677-1269
11-digit billing NDC 70677126901
NCPDP billing unit GM — per gram (weight)
RxCUI 1298448
UNII R8XA2029ZI
Application # ANDA205181
SPL Set ID b4913a89-56fd-4710-b28e-6fb6d50fd3f3
Established class (EPC) Benzylamine Antifungal
Chemical class Benzylamines
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-11-07
Route TOPICAL
Dosage form CREAM
Substance BUTENAFINE HYDROCHLORIDE

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GCN Seq No 029333
GCN 37521
HICL code 012258
Ingredient (HICL) Butenafine Hcl
HIC1 code Q
Therapeutic class — broad (HIC1) Ear/Eye/Nose/Rectum/Topical/Vagina/Other
HIC2 code Q5
Therapeutic class — intermediate (HIC2) Agents Acting Principally On The Skin
HIC3 code Q5F
Therapeutic class — specific (HIC3) Topical Antifungals
AHFS code 84:04.08.12
AHFS class Benzylamines (Skin And Mucous Membrane)
FDB label name FT ATHLETE'S FOOT 1% CREAM
FDB brand name Athlete's Foot
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 029333
  • GCN: 37521
  • HICL (First Databank): 012258
  • AHFS class code: 84:04.08.12
  • RxCUI (RxNorm): 1298448
Why two NDCs? The FDA registers this code as 70677-1269-1 — a 5-4-1 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 package segment → 70677-1269-01. 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 Benzylamine Antifungal class.

Pharmacologic class Benzylamine Antifungal
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

Label name FT ATHLETE'S FOOT 1% CREAM Ingredient Butenafine Hcl
📗 Our plain-language guide HelloPharmacist
  • It treats fungal skin infections. Depending on the product, that means athlete's foot between the toes, jock itch and ringworm. It also relieves itching, burning, cracking and scal...
  • Wash the area with soap and water and dry it completely. Then apply the cream as your product directs. Wash your hands afterward. Jock itch and ringworm are usually once a day for...
  • On products labeled for athlete's foot, the directions are twice a day for 1 week or once a day for 4 weeks, or as your doctor directs. Wear well-fitting, ventilated shoes and chan...
  • How long do I use it for athlete's foot?
📖 Read our full Butenafine guide →

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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 gPer package
Retail pharmacies payNADAC · weekly $0.307 $9.21 / 30 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
Dec 2025 Mar 2026 Jun 2026 Sep 2026 $0.313 $0.304
Flat over the last 10 months.
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
70677-1269-01 You're viewing this Main listing 1 TUBE in 1 CARTON / 30 g in 1 TUBE 2024-11-07 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Athletes Foot 10 mg/gthis 70677-1269-01 STRATEGIC 1 tube $0.307 — Availability likely —
Athletes Foot 10 mg/g 00363-2100-02 Walgreen 1 tube — — FDA listed —
Jock Itch 10 mg/g 00363-2101-08 Walgreen 1 tube — — FDA listed —
Lotrimin Ultra 1 g/100g 11523-0082-01 Bayer 1 tube — — FDA listed —
Lotrimin Ultra Ringworm 1 g/100g 11523-0158-02 Bayer 1 tube — — FDA listed —
Lotrimin Ultra Athletes Foot 1 g/100g 11523-4338-01 Bayer 1 tube — — FDA listed —
Lotrimin Ultra Jock Itch 1 g/100g 11523-4339-01 Bayer 1 tube — — FDA listed —
Athletes Foot 10 mg/g 11673-0016-02 Target 1 tube — — FDA listed —
Jock Itch Cream 10 mg/g 11673-0436-01 TARGET 1 tube — — FDA listed —
Athletes Foot 10 mg/g 11822-2100-02 Rite 1 tube — — FDA listed —
Butenafine Hydrochloride 10 mg/g 21130-0965-01 Albertsons 1 tube — — FDA listed —
Butenafine Hydrochloride Athletes Foot 10 mg/g 30142-0210-02 Kroger 1 tube — — FDA listed —
Athletes Foot 10 mg/g 36800-0049-01 TOPCO 1 tube — — FDA listed —
Athletes Foot Ultra 10 mg/g 37808-0013-02 H 1 tube — — FDA listed —
Butenafine Hydrochloride Jock Itch 10 mg/g 49035-0178-08 Wal-Mart 1 tube — — FDA listed —
Athletes Foot Ultra 10 mg/g 49035-0225-08 Wal-Mart 1 tube — — FDA listed —
Athletes Foot 10 mg/g 51672-2100-01 Sun 1 tube — — FDA listed —
Jock Itch 10 mg/g 51672-2101-01 Sun 1 tube — — FDA listed —
Athletes Foot 10 mg/g 69842-0986-02 CVS 1 tube — — FDA listed —
Butenafine Hydrochloride 1% 10 mg/g 69842-0989-08 CVS 1 tube — — FDA listed —
Butenafine Hydrochloride 10 mg/g 73581-0210-02 YYBA 1 tube — — FDA listed —
Butenafine Hydrochloride 10 mg/g 79481-0086-01 MEIJER 1 tube — — FDA listed —
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
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

🏛️
2024
On the market since
Nov 2024
📍
2026
Currently FDA-listed
2 years listed
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

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 LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
  • UNII 495CTZ441V
    Ceteth-23 is a synthetic emulsifier made by combining cetyl alcohol with ethylene oxide. It helps mix oil and water in liquid formulations and improves how the medicine spreads on skin or is absorbed.
  • UNII 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII FCZ5MH785I
    A waxy substance made from glycerin and stearic acid. It works as an emulsifier to help mix oil and water ingredients together, and as a thickener to give the medicine its proper texture and consistency.
  • UNII 581437HWX2
    A synthetic oily liquid made from propylene glycol and fatty acids. It works as an emollient and solubilizer in medicines, helping dissolve active ingredients and improve how the product spreads or absorbs.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • UNII 9O3K93S3TK
    Trolamine is an alkaline compound used as a pH buffer and emulsifier in medicines. It helps neutralize acids, stabilize formulations, and enable mixing of oil and water-based ingredients.
  • 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.
  • UNII B6E5W8RQJ4
    White petrolatum is a purified mineral oil product used as a lubricant and skin protectant in medications. It helps pills slide through manufacturing equipment and can soften or protect the skin when applied topically.

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

The official label also statesbenzyl alcohol, cetyl alcohol, glycerin, glyceryl monostearate SE, polyoxyethylene (23) cetyl ether, propylene glycol dicaprylate, purified water, sodium benzoate, stearic acid, trolamine, white petrolatum

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

LabelerSTRATEGIC SOURCING SERVICES LLC
Application holderSUN PHARMA CANADA INC
FDA applicationANDA205181 (ANDA)
Labeler code70677
First marketedNov 2024
Product typeHuman Otc Drug
Portfolio316 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 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 34 words ▾

Uses cures most athlete's foot between the toes. Effectiveness on the bottom or sides of foot is unknown. cures most jock itch and ringworm relieves itching, burning, cracking, and scaling which accompany these conditions

⏱️ Dosage and Administration 135 words ▾

Directions adults and children 12 years and older: use the tip of the cap to break the seal and open the tube wash the affected skin with soap and water and dry completely before applying for athlete's foot between the toes: apply to affected skin between and around the toes twice a day for 1 week (morning and night), or once a day for 4 weeks, or as directed by a doctor. Wear well-fitting, ventilated shoes. Change shoes and socks at least once daily. for jock itch and ringworm: apply once a day to affected skin for 2 weeks or as directed by a doctor.

Apply between and around the toes 1 week twice a day or 4 weeks once a day wash hands after each use children under 12 years: ask a doctor Image

⚠️ Warnings 76 words ▾

Warnings For external use only Do not use on nails or scalp in or near the mouth or the eyes for vaginal yeast infections When using this product do not get into the eyes. If eye contact occurs, rinse thoroughly with water. Stop use and ask a doctor if too much irritation occurs or irritation gets worse Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 24 words ▾

Other information do not use if seal on tube is broken or not visible store between 20° to 25° C (68° to 77° F)

🧪 Active Ingredient 5 words ▾

Active ingredient Butenafine hydrochloride 1%

🧪 Inactive Ingredients 26 words ▾

Inactive ingredients benzyl alcohol, cetyl alcohol, glycerin, glyceryl monostearate SE, polyoxyethylene (23) cetyl ether, propylene glycol dicaprylate, purified water, sodium benzoate, stearic acid, trolamine, white petrolatum

🎯 Purpose 2 words ▾

Purpose Antifungal

📄 Do Not Use 19 words ▾

Do not use on nails or scalp in or near the mouth or the eyes for vaginal yeast infections

📄 When Using This Product 18 words ▾

When using this product do not get into the eyes. If eye contact occurs, rinse thoroughly with water.

📄 Stop Use and Ask a Doctor If 15 words ▾

Stop use and ask a doctor if too much irritation occurs or irritation gets worse

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 3 words ▾

Questions? call 833-358-6431

📄 Package Label / Principal Display Panel 35 words ▾

PRINCIPAL DISPLAY PANEL - 30 g Tube Carton Foster & Thrive™ PRESCRIPTION STRENGTH Athlete's Foot Cream Butenafine Hydrochloride Cream 1% ANTIFUNGAL NET WT 1 OZ (30 g) PRINCIPAL DISPLAY PANEL - 30 g Tube Carton

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Athletes Foot (this brand).

Top reported reactions

Nausea910
Pain881
Headache814
Macular Degeneration812
Dyspnoea802
Fatigue731
Diarrhoea677

Age at onset

Neonate47
Infant20
Child41
Adolescent25
Adult1,316
Elderly1,057

Reporter sex

14,249 reports
Male · 35%
Female · 65%
Unknown · 0%

Serious outcomes

Hospitalization4,634
Death1,070
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 1,101 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
← 70677-1268-01 · Strategic 70677-1270-01 · Strategic →
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.