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CheeZheng Pain Relieveing Plaster camphor 1 g/100g Plaster, 1.2 g — NDC 66506-0183-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

CheeZheng Pain Relieveing Plaster camphor 1 g/100g Plaster, 1.2 g — NDC 66506-183-01 (Billing 66506-0183-01)

by Tibet Cheezheng Tibetan Medicine Co. Ltd. · 5 PACKAGE in 1 PACKAGE / 1.2 g in 1 PACKAGE

This is a package of 1.2 g of CheeZheng Pain Relieveing Plaster camphor 1 g/100g Plaster from Tibet Cheezheng Tibetan Medicine Co. Ltd., marketed since Nov 2019 and currently FDA-listed. It is this product's only package size.

NDC 66506-0183-01
🏷️ FDA NDC (as labeled) 66506-183-01 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 66506-183-01
Product NDC 66506-183
11-digit billing NDC 66506018301
RxCUI 1725038
UNII N20HL7Q941
Application # M017
SPL Set ID abcebdf1-9037-4094-93e1-ce8f20b18ea7
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-11-29
Route TOPICAL
Dosage form PLASTER
Substance CAMPHOR (NATURAL)
Quick answers
  • RxCUI (RxNorm): 1725038
Why two NDCs? The FDA registers this code as 66506-183-01 — 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 → 66506-0183-01. 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.

Clinical

🧪 What is this product?

CheeZheng Pain Relieving Plaster is a topical patch containing camphor, a natural ingredient commonly used 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 products rather than as an individually reviewed application. Camphor is typically used in such plasters to provide localized warming or cooling sensations that may help temporarily ease minor aches and pains when applied to the skin.

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.
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
66506-0183-01 You're viewing this Main listing 5 PACKAGE in 1 PACKAGE / 1.2 g in 1 PACKAGE 2019-11-29 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
CheeZheng Pain Relieveing Plaster 1 g/100gthis 66506-0183-01 Tibet 1.2 g — — FDA listed —
Tibetree Pain Relieveing Medicated Plaster 1 g/100g 66506-0186-01 Tibet 1.2 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

🏛️
2019
On the market since
Nov 2019
📍
2026
Currently FDA-listed
7 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 B86IS274O0
    A plant extract from safflower flower buds used as a natural colorant and flavoring agent in medicines. It provides color and taste to make the product more appealing.
  • UNII W5488JUO8U
    A plant extract from turmeric root used as a natural colorant and flavoring agent in medicines. It provides yellow-to-orange color and mild spice flavor to tablets, capsules, and liquids.
  • UNII 4C36LPC9I2
    A plant extract from myricaria paniculata stem used as a natural colorant or flavoring agent in medications. It may also function as an antioxidant to help preserve the medicine's stability.
  • UNII 7276D7W5GN
    Oxytropis falcata whole is a plant material used as a filler or bulking agent in some formulations. It helps add volume and structure to the medicine while serving no known active therapeutic role.
  • UNII 7CEU5N8573
    A plant extract from Phlomoides rotata used as a natural flavoring or aromatic ingredient in medicines to improve taste or aroma.
  • UNII K447936H97
    A plant extract from the fruit rind of Zanthoxylum bungeanum, commonly used as a flavoring or aromatic agent in medicines to improve taste or add sensory characteristics to the product.

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

The official label also statesZanthoxylum bungeanum Maxim, Lamiophlomis rotata (Benth.) Kudo, Curcuma longa L, Carthamus tinctorius L, Myricaria germanica (L.) Desv, Oxytropis falcata Bunge

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 marketedNov 2019
Product typeHuman Otc Drug
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 8 words ▾

Uses For the temporary relief of minor pain.

⏱️ Dosage and Administration 85 words ▾

Directions ■Adults and children 12 years of age and older: remove protective film from the plaster, pour the liquid onto the pad of plaster and apply it to the painful area or acupoint as directed (see figure) ■Use 1 to 2 plasters every 24 hours ■Apply the plaster to the affected area for 4 to 8 hours ■Do not apply to area with excessive hair. Adhesive plaster 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 1%.................……….…….External analgesic

🧪 Inactive Ingredients 22 words ▾

Inactive ingredients Zanthoxylum bungeanum Maxim, Lamiophlomis rotata (Benth.) Kudo, Curcuma longa L, Carthamus tinctorius L, Myricaria germanica (L.) Desv, Oxytropis falcata Bunge

🎯 Purpose 3 words ▾

Purpose External analgesic

📄 Do Not Use 11 words ▾

Do not use on wounds irritated or damaged skin sensitive skin

📄 Ask a Doctor Before Use If 7 words ▾

Do not use otherwise than as directed

📄 When Using This Product 27 words ▾

When using this product avoid contact with the eyes do not use more than 2 plasters a day do not use 1 hour before or after bathing

📄 Stop Use and Ask a Doctor If 35 words ▾

Stop use and ask a doctor if Condition worsens Symptoms persist for more than 7 days Symptoms clear up and occur again within a few days Eexcessive irritation of the skin develops Redness is present

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant If pregnant, ask a health professional before use

📄 Keep Out of Reach of Children 16 words ▾

Keep out of reach of children Keep out of reach of children to avoid accidental poisoning

📄 Other Information 13 words ▾

Other information Store at room temperature, 10 ℃ to 30℃ (50℉ to 86℉)

📄 Questions or Comments 2 words ▾

Questions? +1-888-915-6789

📄 Package Label / Principal Display Panel 29 words ▾

CHEEZHENG PRP OUTER BOX CHEEZHENG PRP BOX InnerPackage INNER LIQ BAG CHEEZHENG PRP INNER BAG CHEEZHENG PRP BAG

InnerPackage INNER LIQ BAG

CHEEZHENG PRP INNER BAG CHEEZHENG PRP BAG

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 CheeZheng Pain Relieveing Plaster (this brand).

Top reported reactions

Fatigue30
Drug Hypersensitivity29
Pain29
Pruritus26
Headache24
Pneumonia24
Dyspnoea23

Reporter sex

167 reports
Male · 39%
Female · 61%

Serious outcomes

Hospitalization76
Disabling4
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 32 0
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.
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.
← 66503-0001-01 · Johnson 66506-0184-01 · Tibet →
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.