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Mqupin Knee Patch 1.5 g/1001; 1.2 g/1001 Patch, 100 patches — NDC 83781-0002-05 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Mqupin Knee Patch 1.5 g/1001; 1.2 g/1001 Patch, 100 patches — NDC 83781-002-05 (Billing 83781-0002-05)

by Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd · 100 PATCH in 1 BOX

This is a package of 100 patches of Mqupin Knee Patch 1.5 g/1001; 1.2 g/1001 Patch from Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd, marketed since Nov 2023 and currently FDA-listed.

NDC 83781-0002-05
🏷️ FDA NDC (as labeled) 83781-002-05 billing pads the product segment with a zero
This package
Contains100 patches Pack sizes5 compare ↓
Product page 83781-0002-01 Also comes in: 14 patches 83781-002-01 28 patches 83781-002-02 42 patches 83781-002-03 64 patches 83781-002-04
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 27, 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 83781-002-05 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
83781 labeler · 002 product · 05 package
Package marketed since
Nov 5, 2023
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
6973634830746
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 83781-002-05
Product NDC 83781-002
11-digit billing NDC 83781000205
UNII 5TJD82A1ET, M89NIB437X
UPC 6973634830746
Application # M017
SPL Set ID 09772e4b-8193-3771-e063-6394a90a9516
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-11-05
Route TOPICAL
Dosage form PATCH
Substance CAMPHOR (SYNTHETIC); BORNEOL
Why two NDCs? The FDA registers this code as 83781-002-05 — 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 → 83781-0002-05. 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

🧪 What is this product?

Mqupin Knee Patch is a topical patch containing borneol and synthetic camphor, which are commonly used as counterirritants in over-the-counter pain-relief products. This is an OTC monograph drug, meaning it is marketed under FDA's established rules for this category of topical analgesic patches rather than as an individually reviewed application. The patch is typically used to deliver these ingredients through the skin to the area being treated.

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 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: 14 patches 28 patches 42 patches 64 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
83781-0002-01 83781-002-01 Main listing 14 PATCH in 1 BOX 2023-11-05 — Active
83781-0002-02 83781-002-02 28 PATCH in 1 BOX 2023-11-05 — Active
83781-0002-03 83781-002-03 42 PATCH in 1 BOX 2023-11-05 — Active
83781-0002-04 83781-002-04 64 PATCH in 1 BOX 2023-11-05 — Active
83781-0002-05 You're viewing this 100 PATCH in 1 BOX 2023-11-05 — Active

You're viewing the largest of 5 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 100 patches — 100 patch in 1 box.
How does this package differ from NDC 83781-0002-01?
Both are Mqupin Knee Patch 1.5 g/1001; 1.2 g/1001 Patch — the drug itself is identical. This page's package is the 100 patches one, while NDC 83781-0002-01 is the 14 patches package.
What NDC number is used to bill for this package of Mqupin Knee Patch 1.5 g/1001; 1.2 g/1001 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
MQUPIN Knee Patch 1.5 g/1001; 1.2 g/1001 83781-0011-01 Zhengzhou 24 patches — — FDA listed —
Mqupin Knee Patch 1.5 g/1001; 1.2 g/1001this 83781-0002-05 Zhengzhou 100 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

🏛️
2023
On the market since
Nov 2023
📍
2026
Currently FDA-listed
3 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 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 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 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 C5529G5JPQ
    Ginger is a plant-derived ingredient used as a flavoring agent to add taste and aroma to medicines. It may also provide mild soothing properties to support product palatability.
  • UNII 4VA0BH57HU
    A plant extract from osmanthus flowers used as a natural flavor and fragrance ingredient in medicines. It adds pleasant taste and aroma to make the product more acceptable to take.
  • UNII E849G4X5YJ
    Saffron is a natural spice derived from the crocus flower. It functions as a colorant and flavoring agent, giving medicines a yellow to orange hue and subtle taste.
  • UNII F84709P2XV
    Wormwood is a plant extract used as a flavoring agent in medicines. It provides a bitter taste to help mask other flavors or make the medication easier to take.

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

The official label also statesDried ginger, saffron, Wormwood, mugwort oil, osmanthus flower oil, eucalyptus leaf oil, cinnamon.

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

LabelerZhengzhou Miaoqi Pharmaceutical Technology Co., Ltd
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code83781
First marketedNov 2023
Product typeHuman Otc Drug
Portfolio7 products on file

More NDCs from Zhengzhou Miaoqi Pharmaceutical Technology Co.,... labeler code 83781

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 📄 Ask a Doctor Before Use If 📄 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 15 words ▾

Use temporarily relieves minor pain associated with: ■arthritis ■muscle strains ■sprains ■bruises ■ joint pain

⏱️ Dosage and Administration 37 words ▾

Directions

Directions adults and children over 12 years: ■clean and dry the affected area ■remove backing from patch and apply patch to affected area ■use 1 patch per knee for 8 to 12 hours, once per day

⚠️ Warnings 5 words ▾

Warnings For external use only.

📦 Storage and Handling 11 words ▾

Other information store at room temperature, not to exceed 86°F (30°C)

🧪 Active Ingredient 6 words ▾

Active Ingredient Borneol 1.2% Camphor 1.5%

🧪 Inactive Ingredients 15 words ▾

Inactive ingredients Dried ginger, saffron, Wormwood, mugwort oil, osmanthus flower oil, eucalyptus leaf oil, cinnamon.

🎯 Purpose 3 words ▾

Purpose Topical Analgesic

📄 Ask a Doctor Before Use If 7 words ▾

Ask Doctor children 12 years or younger

📄 When Using This Product 50 words ▾

When Using ■ use only as directed ■ do not bandage tighty or use with a heating pad ■ avoid contact with eyes and mucous membranes ■ do not apply to wounds or damaged, broken or imitated skin ■ do not use at the same time as other topical analgesics

📄 Stop Use and Ask a Doctor If 63 words ▾

Stop Use ■ rash, itching or excessive skin irritation develops ■ condition worsens ■ symptoms persist for more than 7 days ■ symptoms clear up and occur again within a few days If pregnant or breastfeeding, 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

📄 Keep Out of Reach of Children 12 words ▾

Keep Out Of Reach Of Children Keep Out Of Reach Of Children

📄 Questions or Comments 2 words ▾

Questions [email protected]

📄 Package Label / Principal Display Panel 4 words ▾

PRINCIPAL DISPLAY PANEL 1

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 Zhengzhou Miaoqi Pharmaceutical Technology 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 4 other package presentations of this same product, including 14 patches (83781-0002-01), 28 patches (83781-0002-02), 42 patches (83781-0002-03). 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?
Zhengzhou Miaoqi Pharmaceutical Technology 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.
← 83781-0001-01 · Zhengzhou 83781-0003-01 · Zhengzhou →
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.