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Tibetree Cheezheng Joint Analgesic Patch camphor 3 g/100g Patch, 2 patches — NDC 66506-0188-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Tibetree Cheezheng Joint Analgesic Patch camphor 3 g/100g Patch, 2 patches — NDC 66506-188-02 (Billing 66506-0188-02)

by Tibet Cheezheng Tibetan Medicine Co. Ltd · 2 PATCH in 1 PACKET / 1.7 g in 1 PATCH

This is a package of 2 patches of Tibetree Cheezheng Joint Analgesic Patch camphor 3 g/100g Patch from Tibet Cheezheng Tibetan Medicine Co. Ltd, marketed since Jun 2024 and currently FDA-listed.

NDC 66506-0188-02
🏷️ FDA NDC (as labeled) 66506-188-02 billing pads the product segment with a zero
This package
Contains2 patches Pack sizes4 compare ↓
Product page 66506-0188-01 Also comes in: 2 patches 66506-188-04 3 patches 66506-188-01 3 patches 66506-188-03
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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 66506-188-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
66506 labeler · 188 product · 02 package
Package marketed since
Jun 10, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0850064250114, 0850064250077, 0850064250084, 0850064250107
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 66506-188-02
Product NDC 66506-188
11-digit billing NDC 66506018802
RxCUI 1603829
UNII N20HL7Q941
UPC 0850064250114, 0850064250077, 0850064250084, 0850064250107
Application # M017
SPL Set ID 65a8a63f-1864-473e-be72-7840a6a5dee7
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-06-10
Route TOPICAL
Dosage form PATCH
Substance CAMPHOR (NATURAL)
Quick answers
  • RxCUI (RxNorm): 1603829
Why two NDCs? The FDA registers this code as 66506-188-02 — 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 → 66506-0188-02. 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?

Tibetree Cheezheng Joint Analgesic Patch is a topical patch containing camphor, a natural ingredient. This product is marketed as an over-the-counter monograph drug, meaning it follows established FDA rules for its category rather than undergoing individual application review. Camphor is typically used in topical products for its warming and cooling sensations, and is commonly found in patches and creams intended for localized discomfort relief.

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: 2 patches 3 patches 3 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
66506-0188-01 66506-188-01 Main listing 3 PATCH in 1 BOX / 1.7 g in 1 PATCH 2024-06-11 — Active
66506-0188-02 You're viewing this 2 PATCH in 1 PACKET / 1.7 g in 1 PATCH 2024-06-10 — Active
66506-0188-03 66506-188-03 3 PATCH in 1 BOX / 1.7 g in 1 PATCH 2024-06-10 — Active
66506-0188-04 66506-188-04 2 PATCH in 1 PACKET / 1.7 g in 1 PATCH 2024-06-10 — Active

Pack size FAQ

What quantity is in this package?
This package contains 2 patches — 2 patch in 1 packet / 1.7 g in 1 patch.
How does this package differ from NDC 66506-0188-04?
Both are Tibetree Cheezheng Joint Analgesic Patch camphor 3 g/100g Patch — the drug itself is identical. This page's package is the 2 patches one, while NDC 66506-0188-04 is the 2 patches package.
What NDC number is used to bill for this package of Tibetree Cheezheng Joint Analgesic Patch camphor 3 g/100g 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
Tibetree Cheezheng Joint Analgesic Patch 3 g/100gthis 66506-0188-02 Tibet 2 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

🏛️
2024
On the market since
Jun 2024
📍
2026
Currently FDA-listed
2 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 427F13FDK8
    Aconitum pendulum root is a plant-derived ingredient used as a flavoring or traditional component in some herbal formulations. It functions to add taste or support the product's botanical profile.
  • 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 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 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 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 88S87KL877
    Rosin is a sticky resin extracted from pine trees. It's used in medicines as a binder and adhesive to help hold tablet ingredients together and improve how the medicine sticks to surfaces.
  • 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.

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

The official label also statesAconitum Pendulum Radix. Borneolum Syntheticum, Methyl salicylate, Rubber, Zinc Oxide, Lanolin, Petroleum, Rosin

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

LabelerTibet Cheezheng Tibetan Medicine Co. Ltd
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code66506
First marketedJun 2024
Product typeHuman Otc Drug
Portfolio3 products on file

More NDCs from Tibet Cheezheng Tibetan Medicine Co. Ltd labeler code 66506

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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 7 words ▾

Uses For the temporary relief of pains

⏱️ Dosage and Administration 71 words ▾

Directions Adults and children 12 years of age and older: remove protective film from the patch and apply it to the painful area Use 1 to 2 plasters every 24 hours Apply the patch to the affected area for 4 to 8 hours Do not apply to area with excessive hair. Adhesive patch may hurt skin upon removal. Children under 12 years of age: do not use or consult a doctor

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 5 words ▾

Active ingredients Camphor 3%.................……….…….External analgesic

🧪 Inactive Ingredients 15 words ▾

Inactive ingredients Aconitum Pendulum Radix. Borneolum Syntheticum, Methyl salicylate, Rubber, Zinc Oxide, Lanolin, Petroleum, Rosin

🎯 Purpose 3 words ▾

Purpose External analgesic

📄 Do Not Use 14 words ▾

Do not use on irritated or damaged skin sensitive skin if allergic to plaster

📄 Ask a Doctor Before Use If 7 words ▾

Do not use otherwise than as directed

📄 When Using This Product 13 words ▾

When using this product Avoid contact with the eyes or on mucous membrane

📄 Stop Use and Ask a Doctor If 35 words ▾

Stop use and ask a doctor if Condition worsens Symptoms persist for more than 3 days Symptoms clear up and occur again within a few days Excessive irritation of the skin develops Redness is present

🤰 If Pregnant or Breast-Feeding 15 words ▾

If pregnant If pregnant, breast feeding, glaucoma, prostate hypertrophy, ask a health professional before use

📄 Keep Out of Reach of Children 29 words ▾

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

📄 Other Information 11 words ▾

Other information store at room temperature, 10° to 30°C(50°F to 86°F)

📄 Questions or Comments 2 words ▾

Questions? 1-888-915-6789

📄 Package Label / Principal Display Panel 36 words ▾

Tibetree Cheezheng Joint Analgesic Patch PDP Cheezheng Joint Analgesic Patch Bilingual Outer Box Cheezheng Joint Analgesic Patch Bilingual Inner Pkg Tibetree Cheezheng Joint Analgesic Patch English Outer Box Tibetree Cheezheng Joint Analgesic Patch English Inner Pkg

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 Tibetree Cheezheng Joint Analgesic Patch (this brand).

Top reported reactions

Fatigue30
Drug Hypersensitivity29
Pain29
Pruritus26
Headache24
Pneumonia24
Dyspnoea23

Age at onset

Neonate1
Infant1
Adolescent1
Adult19
Elderly16

Reporter sex

167 reports
Male · 39%
Female · 61%

Serious outcomes

Hospitalization76
Life-threatening9
Disabling4
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 32 2
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.

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 Tibet Cheezheng Tibetan Medicine 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 3 other package presentations of this same product, including 2 patches (66506-0188-04), 3 patches (66506-0188-01), 3 patches (66506-0188-03). 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?
Tibet Cheezheng Tibetan Medicine 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.
← 66506-0186-01 · Tibet 66507-0001-01 · Zhejiang →
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.