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Nufabrx Knee Sleeve Capsaicin .25 g/100g Cloth, 1 g — NDC 72490-0044-10 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Nufabrx Knee Sleeve Capsaicin .25 g/100g Cloth, 1 g — NDC 72490-044-10 (Billing 72490-0044-10)

by Nufabrx LLC · 1 g in 1 BOX

This is a package of 1 g of Nufabrx Knee Sleeve Capsaicin .25 g/100g Cloth from Nufabrx LLC, marketed since Dec 2025 and currently FDA-listed. It is this product's only package size.

NDC 72490-0044-10
🏷️ FDA NDC (as labeled) 72490-044-10 billing pads the product segment with a zero
OTC 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

NDC database record

One package, one record: these facts belong to NDC 72490-044-10 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
72490 labeler · 044 product · 10 package
Package marketed since
Dec 30, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 7249004410 0
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 72490-044-10
Product NDC 72490-044
11-digit billing NDC 72490004410
UNII S07O44R1ZM
Application # M017
SPL Set ID 473098ca-02f1-c287-e063-6394a90a37e1
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-12-30
Route TOPICAL
Dosage form CLOTH
Substance CAPSAICIN
Why two NDCs? The FDA registers this code as 72490-044-10 — 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 → 72490-0044-10. 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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • Yes, completely normal — and it actually means the medicine is working. Capsaicin activates the same pain-sensing receptors in your skin that respond to heat and spicy food. That b...
  • Why does capsaicin burn when I put it on? Is that normal?
  • For most OTC creams and ointments, you can apply up to 3 to 4 times a day. For OTC patches, apply to clean, dry skin and remove after no more than 8 hours — again, up to 3 to 4 tim...
  • How often should I apply capsaicin cream or use the patch?
📖 Read our full Capsaicin guide →

Supplement & herbal interactions

Some supplements/herbs that may interact with Capsaicin (prescription drug) — tap one for details:

Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor
🌿 Every supplement checked against Capsaicin (prescription drug) (3 interactions) — ranked by severity →
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 eachPer 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
72490-0044-10 You're viewing this Main listing 1 g in 1 BOX 2025-12-30 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Capsadyn .25 g/100g 83009-0169-01 Chorda 28 g — — FDA listed —
Nufabrx Knee Sleeve .25 g/100gthis 72490-0044-10 Nufabrx 1 g — — FDA listed —
Nufabrx Shin Sleeve .25 g/100g 72490-0045-10 Nufabrx 1 g — — FDA listed —
Nufabrx Ankle Sleeve .25 g/100g 72490-0046-10 Nufabrx 1 g — — FDA listed —
Nufabrx Medicine Infused Ankle Sleeve .25 g/100g 72490-0039-10 Nufabrx 1 g — — FDA listed —
Nufabrx Medicine Infused Wrist Sleeve .25 g/100g 72490-0040-10 Nufabrx 1 g — — FDA listed —
Nufabrx Arm Sleeve .25 g/100g 72490-0041-10 Nufabrx 1 g — — FDA listed —
Nufabrx Elbow Sleeve .25 g/100g 72490-0042-10 Nufabrx 1 g — — FDA listed —
Astrapharm Chilli Brand .25 g/100g 11993-0000-01 Dersan 24 patches — — FDA listed —
Nufabrx Medicine Infused Elbow Sleeve .25 g/100g 72490-0038-10 Nufabrx 1 g — — FDA listed —
Nufabrx Leg Sleeve .25 g/100g 72490-0043-10 Nufabrx 1 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

🏛️
2025
On the market since
Dec 2025
📍
2026
Currently FDA-listed
1 year 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.

🧪 Avoiding an ingredient? See Capsaicin inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII U73D397055
    A blend of plant-derived fats and oils that act as a liquid carrier and solvent in medicines. It helps dissolve active ingredients and improve how the body absorbs them from capsules or liquid formulations.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also statescaprylic/capric triglyceride

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

LabelerNufabrx LLC
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code72490
First marketedDec 2025
Product typeHuman Otc Drug
Portfolio17 products on file

More NDCs from Nufabrx LLC labeler code 72490

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 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 17 words ▾

Uses Temporary relieves of minor pain associated with: arthritis, knee pain, muscle strains, sprains, bruises and cramps.

⏱️ Dosage and Administration 18 words ▾

Directions Clean and dry affected area Remove sleeve from packaging and place on knee Wash hands after applying

⚠️ Warnings 134 words ▾

Warnings For external use only When using this product use only as directed do not wear if you are allergic to any material in this product or chili peppers do not apply to wounds, damaged or irritated skin do not get into eyes or on mucous membranes do not use with heating pad or other external analgesic products a slight burning sensation may occur upon application in some cases if severe burning sensation occurs, discontinue use immediately Stop use and ask doctor if Condition worsens severe skin irritation occurs pain persists more than 7 days symptoms clear up and occur again within a few days If pregnant or beastfeeding ask a health professional before use.

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

📦 Storage and Handling 39 words ▾

Product Care instructions machine wash cold, separately, gentle cycle, mild detergent, tumble dry low do not bleach, do not iron, do not dry clean do not store in direct sunlight, protect product from excessive moisture when not in use

🧪 Active Ingredient 4 words ▾

Active Ingredient Capsaicin 0.25%

🧪 Inactive Ingredients 4 words ▾

Inactive ingredients caprylic/capric triglyceride

🎯 Purpose 3 words ▾

Purpose Topical Analgesic

📄 Do Not Use 72 words ▾

When using this product use only as directed do not wear if you are allergic to any material in this product or chili peppers do not apply to wounds, damaged or irritated skin do not get into eyes or on mucous membranes do not use with heating pad or other external analgesic products a slight burning sensation may occur upon application in some cases if severe burning sensation occurs, discontinue use immediately

📄 Stop Use and Ask a Doctor If 28 words ▾

Stop use and ask doctor if Condition worsens severe skin irritation occurs pain persists more than 7 days symptoms clear up and occur again within a few days

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant or beastfeeding ask a health professional before use.

📄 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.

📄 Package Label / Principal Display Panel 4 words ▾

Package Label Entire Label

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 Nufabrx LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Nufabrx 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.
← 72490-0043-10 · Nufabrx 72490-0045-10 · Nufabrx →
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.