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Graphene Far Infrared Herbal Pain Relief Patches Corydalis Rhizome 4 g/100g; 1 g/100g Patch — NDC 84876-0006-01 package photo

Graphene Far Infrared Herbal Pain Relief Patches Corydalis Rhizome 4 g/100g; 1 g/100g Patch

by Changsha Maocheng Trading Co., Ltd · 10 PATCH in 1 BOX (84876-006-01) / 4 g in 1 PATCH
NDC 84876-0006-01
🏷️ FDA NDC (as labeled) 84876-006-01 billing pads the product segment with a zero
This package
Contains4 g in 1 patch Pack sizes2 compare ↓
Also comes in: 10 patches 84876-0006-02
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 →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 84876-006-01
Product NDC 84876-006
11-digit billing NDC 84876000601
UNII 0TUP42692Z, L7T10EIP3A
Application # M017
SPL Set ID 3b604a3c-fe91-7096-e063-6394a90afe04
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-08-01
Route TOPICAL
Dosage form PATCH
Substance CORYDALIS YANHUSUO TUBER; MENTHOL
Why two NDCs? The FDA registers this code as 84876-006-01 — 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 → 84876-0006-01. 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.

🏭 Manufacturer & labeler

LabelerChangsha Maocheng Trading Co., Ltd
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code84876
First marketedAug 2025
Product typeHuman Otc Drug
Portfolio4 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 is this product?

This is a topical patch containing corydalis rhizoma and menthol, marketed as an over-the-counter monograph product under FDA's established rules for this category. Menthol is commonly used in topical pain relief products for its cooling sensation. Corydalis rhizoma is an herbal ingredient that appears in traditional pain relief formulations. The patch is applied to the skin and is typically used to address localized discomfort, though individual results may vary.

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.

🧪 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 5QIU26R6P1
    Achyranthes bidentata root is a plant-derived ingredient used in traditional formulations. It typically functions as a binder or filler to help hold tablet components together and add bulk to the dosage form.
  • UNII 72Q967Y48V
    Artemisia vulgaris oil is a plant-derived essential oil from mugwort. It functions as a flavoring agent and fragrance component in medicines, providing taste or aroma to the formulation.
  • UNII X23X6CW68R
    A plant-derived ingredient from bistorta root, used as a binder and thickening agent to help hold tablet ingredients together and improve the product's consistency and texture.
  • UNII M89NIB437X
    Borneol is a waxy, plant-derived alcohol obtained from camphor trees or made synthetically. It's used in medicines as a flavoring agent and penetration enhancer to improve how active ingredients are absorbed.
  • UNII 5S29HWU6QB
    Cinnamon is a spice derived from tree bark. It's used in medicines as a flavoring agent to improve taste and mask unpleasant flavors, making the medicine easier to take.
  • UNII 3Z927XY19P
    A plant-derived ingredient from Japanese dodder seeds. It acts as a binder and thickening agent to help hold the medicine's components together and achieve the desired consistency in the formulation.
  • UNII LAV5U5022Y
    Methyl salicylate is a naturally derived liquid compound commonly found in wintergreen plants. In medicines, it's used as a flavoring agent and penetrating solvent to help distribute active ingredients evenly throughout topical products.
  • UNII N08U5BOQ1K
    Glucosamine is a natural sugar compound derived from shellfish or made synthetically. In medications, it serves as a humectant and thickening agent to retain moisture and improve texture.
  • UNII 4QQN74LH4O
    Graphite is a form of carbon used as a lubricant and glidant in tablet and capsule manufacturing. It helps powders flow smoothly during production and prevents sticking to equipment.
  • UNII RR83T99U97
    A plant-derived substance from Asian lovage root used in traditional formulations. It may serve as a flavoring agent, fragrance component, or natural additive to support product stability and palatability.
  • UNII H74221J5J4
    Myrrh oil is a fragrant resin extracted from myrrh tree bark. It is used in medicines as a flavoring agent and to add aroma or taste to the product.
  • UNII 90PS6JV9GZ
    A plant-derived ingredient from the Ophiopogon japonicus root, used in traditional medicine formulations. It may serve as a natural filler or consistency agent in herbal preparations.
  • UNII GQX1C1175U
    A plant extract from Panax notoginseng root used in traditional medicine formulations. It may function as a filler or active botanical component in herbal or dietary supplement products.
  • UNII V95R5KMY2B
    Peppermint is a flavoring agent derived from the peppermint plant. It's added to medicines to improve taste and mask bitter or unpleasant flavors, making them easier to take.
  • UNII 05I15JNI2J
    A synthetic polymer that absorbs and holds moisture. Used in tablets and capsules as a super-disintegrant to help the medicine break apart quickly when swallowed, allowing faster drug release.
  • UNII 7YF691N2XM
    A plant extract from jasmine vine stem used as a natural flavoring agent or botanical ingredient. It may help provide taste, aroma, or preserve the formulation in certain medicines.

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

The official label also statesGraphene Fabric Bistort Root Glucosamine Chuanxiong Rhizome Notoginseng Root Mugwort Leaf Peppermint Sodium polyacrylate Achyranthes Root Gaultheria Herb (Wintergreen) Star Jasmine Stem Myrrh Cuscuta Seed Ophiopogon Tuber Cinnamon Bark Borneol

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.

💲 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: 10 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Graphene Far Infrared Herbal Pain Relief Patches 4 g/100g; 1 g/100gthis 84876-0006-01 Changsha 10 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

🏛️
2025
On the market since
Aug 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
84876-0006-01 You're viewing this 10 PATCH in 1 BOX (84876-006-01) / 4 g in 1 PATCH 2025-08-01 Active
84876-0006-02 10 PATCH in 1 BOX (84876-006-02) / 43 g in 1 PATCH 2025-08-01 Active

Pack size FAQ

What quantity is in NDC 84876-0006-01?
NDC 84876-0006-01 is listed by the FDA — 10 patch in 1 box / 4 g in 1 patch.
What NDC number is used to bill for this package of Graphene Far Infrared Herbal Pain Relief Patches Corydalis Rhizome 4 g/100g; 1 g/100g Patch?
Bill NDC 84876-0006-01 — the 11-digit billing format is 84876000601. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 84876-006-01, 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: 84876-0006-01, written without dashes as 84876000601. 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 84876-0006-01, the first segment (84876) is the labeler code FDA assigned to Changsha Maocheng Trading Co., Ltd; the middle segment (0006) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 Changsha Maocheng Trading Co., Ltd. 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 10 patches (84876-0006-02). 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?
Changsha Maocheng Trading Co., Ltd 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 ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 69 words ▾

adults and children 12 years of age and older: Clean and dry affected area, pop apartand partiallypeel back protective film and apply exposed patch to site of pain, Carefullyremove remaining filmwhile pressing the patch to skin and leave in place for up to 8hours. Use on affected area not morethan 3 to 4 times daily.children under 12 years of age: consult a physicianwash hands after use with cool water

⏱️ Dosage and Administration 27 words ▾

Carefullyremove remaining filmwhile pressing the patch to skin and leave in place for up to 8hours. Use on affected area not morethan 3 to 4 times daily.

⚠️ Warnings 3 words ▾

For externaluse only.

🧪 Active Ingredient 5 words ▾

Corydalis Rhizome 4% Menthol 1%

🧪 Inactive Ingredients 30 words ▾

Graphene Fabric Bistort Root Glucosamine Chuanxiong Rhizome Notoginseng Root Mugwort Leaf Peppermint Sodium polyacrylate Achyranthes Root Gaultheria Herb (Wintergreen) Star Jasmine Stem Myrrh Cuscuta Seed Ophiopogon Tuber Cinnamon Bark Borneol

🎯 Purpose 8 words ▾

Temporarily relieves minor aches and pains of muscles

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 84876-0005-01 · Menthol 84876-0101-01 · Changsha →
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.