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Coralite Medicated Heat Capsaicin 249 mg Patch — NDC 65923-0123-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Coralite Medicated Heat Capsaicin 249 mg Patch — NDC 65923-123-01 (Billing 65923-0123-01)

by United Exchange Corp. · 1 PATCH in 1 POUCH / 249 PATCH in 1 PATCH

This is a package of Coralite Medicated Heat Capsaicin 249 mg Patch from United Exchange Corp., marketed since Feb 2016 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 65923-0123-01
🏷️ FDA NDC (as labeled) 65923-123-01 billing pads the product segment with a zero
This package
Contains249 patch in 1 patch Pack sizes2 compare ↓
Main listing for product 65923-123 · Also comes in: 2 patches 65923-123-02
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 65923-123-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
65923 labeler · 123 product · 01 package
Package marketed since
Oct 30, 2018
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6592312301 5
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 65923-123-01
Product NDC 65923-123
11-digit billing NDC 65923012301
RxCUI 1043399
UNII S07O44R1ZM
Application # M017
SPL Set ID a0b89c7e-80bc-43c4-840c-5fd567f60b21
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2016-02-10
Route TOPICAL
Dosage form PATCH
Substance CAPSAICIN
Quick answers
  • RxCUI (RxNorm): 1043399
Why two NDCs? The FDA registers this code as 65923-123-01 — 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 → 65923-0123-01. 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 Capsaicin and similar agents class.

Drug family (ATC) Capsaicin and similar agents, Other local anesthetics
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

Capsaicin topical system is used to treat neuropathic pain from postherpetic neuralgia (PHN; the burning, stabbing pain or aches that may last for months or years after an attack of shingles) or from diabetic neuropathy (numbness or tingling due to nerve damage in people who have diabetes). Capsaicin is a substance that is found in chili peppers. Capsaicin topical system is in a class of medications called topical pain relievers. It works by affecting nerve cells in the skin that are associated with pain, which results in decreased activity of these nerve cells and a reduced sense of pain.

Read the full MedlinePlus article ↗
📗 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.
Try another pack size: 2 patches
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
65923-0123-01 You're viewing this Main listing 1 PATCH in 1 POUCH / 249 PATCH in 1 PATCH 2018-10-30 — Active
65923-0123-02 65923-123-02 2 PATCH in 1 POUCH / 249 PATCH in 1 PATCH 2016-02-10 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 patch in 1 pouch / 249 patch in 1 patch.
What NDC number is used to bill for this package of Coralite Medicated Heat Capsaicin 249 mg Patch?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Good Neighbor Capsaicin Heat Patch for Back .025 g/100g 46122-0753-55 Amerisource 3 patches $1.117 — Availability likely —
Capsaicin Hot Patches .025 g/100g 70000-0556-01 Cardinal 2 patches $1.117 — Availability likely —
Capsimide .025 g/100g 70512-0016-10 Sola 10 pouches $1.117 — Availability likely —
Walgreens Capsaicin Hot Patch .25 mg/g 00363-6691-03 Walgreen 3 patches — — FDA listed —
Capsaicin Heat Patches Back And Large Areas .025 g/100g 00363-9902-03 Walgreen 3 patches — — FDA listed —
WellPatch Warming Pain Relief 25 mg 10742-8127-01 The 1 patch — — FDA listed —
Capsaicin Heat Patches Pain Relief .025 g/100g 11822-4210-03 Rite 3 patches — — FDA listed —
Capsaicin Heat Patches Back And Large Areas .025 g/100g 41250-0842-03 Meijer 3 patches — — FDA listed —
Salonpas-Hot Capsicum .025 g/100g 46581-0700-01 Hisamitsu 1 patch — — Discontinued —
Equate Capsaicin Pain Relieving .25 mg/g 49035-0890-01 Wal-Mart 1 patch — — FDA listed —
Satogesic Hot .25 mg 49873-0608-01 Sato 5 patches — — FDA listed —
Capsaicin .025 g/100g 50488-2025-01 Alexso, 10 patches — — FDA listed —
Capsaicin Heat .025 g/100g 52000-0040-41 Universal 2 patches — — FDA listed —
Solstice Capsaicin Patch Hot .025 g/100g 55614-0410-01 MADISON 1 patch — — FDA listed —
CVS Medicated Heat 1 ct .025 g/g 59779-0770-01 CVS 1 g — — FDA listed —
Best Choice Targeted Warming Capsaicin Heat Patch .025 g/100g 63941-0691-03 Valu 3 patches — — FDA listed —
Coralite Medicated Heat 249 mgthis 65923-0123-01 United 1 patch — — FDA listed —
Coralite Capsaicin Heat Patch 2ct 249 mg/g 65923-0809-02 United 1 patch — — FDA listed —
Capsaicin Pain Relief .702 mg 67510-0303-01 Kareway 1 patch — — FDA listed —
Capsaicin .025 g/100g 69420-7025-01 SA3, 10 patches — — FDA listed —
Capsaicin .025 g/100g 71436-3025-01 ARI 10 patches — — FDA listed —
Pain Relieving Gel-Patch .00025 g/g 73557-0180-05 Shanghai 5 patches — — FDA listed —
BonicaEaseX Hot Capsicum Pain Relieving .25 mg 75568-0042-00 Planet 24 patches — — FDA listed —
Meijer Capsaicin Heat Patch .025 g/100g 79481-0064-03 Meijer 3 patches — — FDA listed —
Capsaicin .025 g/100g 79643-0002-01 PHARMACURE 10 patches — — FDA listed —
Capsaicin 0.025% 2.5 mg/10g 80425-0541-01 Advanced 30 patches — — FDA listed —
CAPSAICIN HEAT Patch .025 g/1001 83559-0013-01 Henan 48 patches — — FDA listed —
Rapid Relief .00025 g/g 83569-0018-06 RAPID 6 patches — — FDA listed —
Honest Med Capsaicin Patch .025 g/100g 84097-0003-24 Proper 24 patches — — FDA listed —
Capsaicin 0.025% 2.5 mg/10g 85096-0401-30 Marcella 30 patches — — FDA listed —
0.025% Capsaicin Pain relief Patch .025 g/100g 85323-0001-00 Xuzhou 5 patches — — FDA listed —
0.025% Capsaicin Pain relief Patch .025 g/100g 85323-0005-01 Xuzhou 48 patches — — 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

🏛️
2016
On the market since
Feb 2016
📍
2026
Currently FDA-listed
10 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 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 TC2D6JAD40
    This is an antihistamine salt form used as an active ingredient in some over-the-counter products. While primarily therapeutic rather than inactive, it may appear in combination formulations where it serves to reduce itching or drowsiness alongside a primary medication.
  • UNII SD112V492J
    Glyceryl rosinate is a sticky substance made by combining rosin (a natural resin from pine trees) with glycerin. It's used in medicines as a binder to help hold solid ingredients together and improve texture and spreadability in certain formulations.
  • UNII 7EV65EAW6H
    Lanolin is a waxy substance derived from sheep's wool. It's used in medicines as an emollient and skin-conditioning agent to soften formulations and improve spreadability in topical products like creams and ointments.
  • UNII 2LQ0UUW8IN
    A natural rubber material derived from the rubber tree. It's used as a coating or component in capsule shells and drug delivery devices to provide structure, flexibility, and controlled release of the medication.
  • UNII 4T6H12BN9U
    Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
  • UNII 7X53O5S2ZY
    Polyisobutylene is a synthetic rubber-like polymer used as a glidant and lubricant in tablet and capsule formulations. It reduces friction between particles and equipment during manufacturing and processing.
  • UNII K7S96QM8DV
    A synthetic rubber-like plastic made from linked chains of styrene and isoprene. It's used in medicines as a binder to hold ingredients together and as a film-former to create protective coatings on tablets or capsules.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
  • UNII SOI2LOH54Z
    Zinc oxide is a white mineral powder used in medicines as a protective barrier agent and color additive. It helps shield skin in topical products and may also serve as a filler or opacifying ingredient.

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

The official label also statesInactive ingredients butylated hydroxytoluene, diphenhydramine, hydrochloride, glyceryl, rosinate, lanolin, natural rubber, petrolatum, polyisobutylene (85,000 MW), styrene-isoprene-styrene block copolymer, titanium dioxide, zinc oxide

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

LabelerUnited Exchange Corp.
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code65923
First marketedFeb 2016
Product typeHuman Otc Drug
Portfolio22 products on file

More NDCs from United Exchange Corp. labeler code 65923

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 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 48 words ▾

Directions adults and children 12 years of age and older: clean and dry affected area remove patch from film apply to affected area no more than 3 to 4 times daily do not wear patch more than 8 hours children under 12 years of age: consult a doctor

⏱️ Dosage and Administration 15 words ▾

Distributed by: United Exchange Corp. 5836 Corporate Ave. Cypress, CA 90630 USA Made in China

⚠️ Warnings 38 words ▾

Warnings For external use only Allergy alert: do not use if you are allergic to capsicum, chili peppers, or any ingredients in this product if prone to allergic reaction from aspirin or salicylates, consult a doctor before use

📦 Storage and Handling 13 words ▾

Other information Avoid storing product in direct sunlight. Protect product from excessive moisture.

🧪 Active Ingredient 8 words ▾

Active ingredient Purpose Capsicum Extract Capsaicin 0.025%..............................Topical Analgesic

🧪 Inactive Ingredients 22 words ▾

Inactive ingredients butylated hydroxytoluene, diphenhydramine, hydrochloride, glyceryl, rosinate, lanolin, natural rubber, petrolatum, polyisobutylene (85,000 MW), styrene-isoprene-styrene block copolymer, titanium dioxide, zinc oxide

🎯 Purpose 21 words ▾

Uses For temporary relief of minor aches and pains of muscles & joints associated with: Simple Backache Arthritis Strains Bruises Sprains

📄 Do Not Use 12 words ▾

Do not use: on wounds or damaged skin. with a heating pad.

📄 When Using This Product 43 words ▾

When using this product: do not use otherwise than directed avoid contact with the eyes, mucous membranes or rashes do not bandage tightly discontinue use at least 1 hour before a bath or shower do not use immediately after a bath or shower

📄 Stop Use and Ask a Doctor If 39 words ▾

stop use and ask a doctor if: condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days redness is present or irritation or rash develops a severe burning sensation occurs

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant or breastfeeding, ask a health professional before use.

📄 Keep Out of Reach of Children 20 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

📄 Package Label / Principal Display Panel 1 words ▾

90198A

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 United Exchange Corp.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 2 patches (65923-0123-02). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
United Exchange Corp. 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.
← 65923-0122-01 · United 65923-0144-57 · United →
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.