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Wu Yang Brand Pain Relieving Medicated Menthol and Camphor 5 g/100g; 3 g/100g Plaster, 10 patches — NDC 55614-0700-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Wu Yang Brand Pain Relieving Medicated Menthol and Camphor 5 g/100g; 3 g/100g Plaster, 10 patches — NDC 55614-700-01 (Billing 55614-0700-01)

by MADISON ONE ACME INC · 10 POUCH in 1 BOX / 1 PATCH in 1 POUCH / 1 g in 1 PATCH

This is a package of 10 patches of Wu Yang Brand Pain Relieving Medicated Menthol and Camphor 5 g/100g; 3 g/100g Plaster from MADISON ONE ACME INC, marketed since Aug 2020 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 55614-0700-01
🏷️ FDA NDC (as labeled) 55614-700-01 billing pads the product segment with a zero
This package
Contains10 patches Pack sizes2 compare ↓
Main listing for product 55614-700 · Also comes in: 1 g 55614-700-02
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 55614-700-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
55614 labeler · 700 product · 01 package
Package marketed since
Aug 31, 2020
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 5561470001 4
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 55614-700-01
Product NDC 55614-700
11-digit billing NDC 55614070001
RxCUI 2393604
UNII L7T10EIP3A, 5TJD82A1ET
Application # M017
SPL Set ID 05c6b95a-aeb6-4234-97c7-8d77eccb38d8
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-08-31
Route TRANSDERMAL
Dosage form PLASTER
Substance MENTHOL; CAMPHOR (SYNTHETIC)
Quick answers
  • RxCUI (RxNorm): 2393604
Why two NDCs? The FDA registers this code as 55614-700-01 — 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 → 55614-0700-01. 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?

This is an over-the-counter medicated plaster containing menthol and synthetic camphor, applied directly to the skin. Menthol and camphor are commonly used together in topical products for their cooling and warming sensations, which are typically included in plasters meant to provide localized relief. This product is marketed as an OTC monograph drug, meaning it follows FDA's established rules for this category of topical pain-relief products rather than being individually reviewed as a new drug application.

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: 1 g
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
55614-0700-01 You're viewing this Main listing 10 POUCH in 1 BOX / 1 PATCH in 1 POUCH / 1 g in 1 PATCH 2020-08-31 — Active
55614-0700-02 55614-700-02 1 PATCH in 1 CANISTER / 1 g in 1 PATCH 2020-12-28 — Active

Pack size FAQ

What quantity is in this package?
This package contains 10 patches — 10 pouch in 1 box / 1 patch in 1 pouch / 1 g in 1 patch.
How does this package differ from NDC 55614-0700-02?
Both are Wu Yang Brand Pain Relieving Medicated Menthol and Camphor 5 g/100g; 3 g/100g Plaster — the drug itself is identical. This page's package is the 10 patches one, while NDC 55614-0700-02 is the 1 patch package.
What NDC number is used to bill for this package of Wu Yang Brand Pain Relieving Medicated Menthol and Camphor 5 g/100g; 3 g/100g Plaster?
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
Icy Hot Pro Pain 180 mg/1; 300 mg 41167-0074-00 Chattem, 5 patches — — FDA listed —
Wu Yang Brand Pain Relieving Medicated 5 g/100g; 3 g/100gthis 55614-0700-01 MADISON 10 patches — — FDA listed —
Icy Hot Pro Pain Relief 180 mg/1; 300 mg 62168-0210-01 Lead 800 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

🏛️
2020
On the market since
Aug 2020
📍
2026
Currently FDA-listed
6 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 1V63N2S972
    A plant extract from angelica dahurica root used in traditional formulations. It may function as a flavoring agent, fragrance component, or natural ingredient to add therapeutic appeal to the medicine.
  • 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 E5GY4I6YCZ
    A fragrant liquid extracted from cinnamon bark, used as a flavoring agent to improve the taste of medicines and make them more pleasant to take.
  • UNII LB1GQP4253
    A plant extract from the teasel root used as a traditional herbal ingredient. In medicines, it may function as a filler or binder to help hold the product together and maintain its form.
  • UNII M3YJ2C28IC
    Dragon's blood is a natural red resin obtained from tropical plants. It's used in medicines as a colorant and binding agent to give pills and capsules their appearance and help hold ingredients together.
  • UNII 731W842X8Q
    A plant extract from the Drynaria fortunei fern root, traditionally used in herbal medicine. In formulations, it may serve as an active botanical ingredient or functional additive, though its specific role depends on the product type.
  • UNII 7CTH8MD549
    A natural plant extract from gardenia fruit used as a colorant in medicines. It provides yellow to orange coloring and may help preserve product stability.
  • 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 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 N6K5787QVP
    Light mineral oil is a clear, odorless liquid derived from petroleum. In medicines, it acts as a lubricant and emollient to help the product spread smoothly and improve texture.
  • UNII 4465L2WS4Y
    A plant extract from Japanese honeysuckle flowers used as a natural flavoring and fragrance ingredient in medicines. It may also help preserve the product and add pleasant taste or aroma.
  • 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 JC71GJ1F3L
    Myrrh is a natural resin obtained from a tree, traditionally used in medicines and perfumes. It may serve as a flavoring agent, fragrance, or mild preservative in formulations.
  • 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 2FN3BA1MZE
    Nepeta tenuifolia flowering top is a plant extract used in herbal formulations. It may serve as a flavoring agent, natural color, or botanical active support ingredient in the product.
  • 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 Y132ZOQ9H7
    A synthetic rubber-like polymer used as a binder and thickening agent in medicines. It helps hold tablet ingredients together and can improve the texture and consistency of formulations.
  • UNII A47JP5ZG9M
    A plant-derived ingredient from rhubarb root. Used as a natural colorant and flavoring agent in medicines, and may help the tablet hold its shape during manufacturing.
  • 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 4VBL71TY4Y
    Safflower is a plant-derived ingredient used as a natural colorant and flavoring agent in medicines. It may also serve as a filler to add bulk to the formulation.
  • UNII 8H84LFK2QD
    A plant root extract used in traditional herbal preparations. It serves as an active botanical ingredient that may provide flavor and natural properties to the formulation.
  • UNII CHL342Y4LA
    A natural extract from acacia wood, used as a binder and astringent in tablets and capsules to help hold ingredients together and improve texture.
  • UNII 4E8QL88U6H
    Taraxacum mongolicum whole is a dried plant material from the dandelion family. It's included as a filler and natural ingredient to add bulk and volume to the formulation.
  • UNII L2CQZ81759
    A plant extract from the root of Zanthoxylum nitidum, a shrub native to Asia. It's used in formulations as a flavoring agent and to support preservation of the medicine.
  • 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.

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

The official label also statesInactive ingredients angelica dahurica root, butylated hydroxytoluene, cinnamon oil, dipsacus asper root, dragon's blood, drynaria fortunei root, gardenia jasminoides fruit, ginger, lanolin, light mineral oil, lonicera japonica flower, methyl salicylate, myrrh, natural latex rubber, nepeta tenuifolia flowering top, petrolatum, polyisobutylene, rheum officinale root, rosin, safflower, saposhnikovia divaricata root, senegalia catechu wood, taraxacum mongolicum whole, zanthoxylum nitidum root and 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

LabelerMADISON ONE ACME INC
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code55614
First marketedAug 2020
Product typeHuman Otc Drug
Portfolio18 products on file

More NDCs from MADISON ONE ACME INC labeler code 55614

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 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 27 words ▾

Uses For the temporary relief of minor aches and pains of muscles and joints due to: ■ arthritis ■ strains ■ simple backache ■ bruises ■ sprains

⏱️ Dosage and Administration 44 words ▾

Directions ■ Adults and children 2 years of age and older: Cut to desired size, remove clear backing, and apply to affected area not more than 3 to 4 times daily. ■ Children under 2 years of age: Do not use, consult a doctor.

⚠️ Warnings 5 words ▾

Warnings For external use only

📦 Storage and Handling 20 words ▾

Other information ■ store at 15º to 30º C (59º to 86º F) in a dry place away from sunlight

🧪 Active Ingredient 6 words ▾

Active ingredients Menthol 5% Camphor 3%

🧪 Inactive Ingredients 60 words ▾

Inactive ingredients angelica dahurica root, butylated hydroxytoluene, cinnamon oil, dipsacus asper root, dragon's blood, drynaria fortunei root, gardenia jasminoides fruit, ginger, lanolin, light mineral oil, lonicera japonica flower, methyl salicylate, myrrh, natural latex rubber, nepeta tenuifolia flowering top, petrolatum, polyisobutylene, rheum officinale root, rosin, safflower, saposhnikovia divaricata root, senegalia catechu wood, taraxacum mongolicum whole, zanthoxylum nitidum root and zinc oxide.

🎯 Purpose 5 words ▾

Purpose External analgesic External analgesic

📄 Do Not Use 28 words ▾

Do not use ■ on wounds ■ on damaged or irritated skin ■ if excessive irritation develops ■ otherwise than as directed, to do so may be dangerous

📄 When Using This Product 18 words ▾

When using this product ■ avoid contact with the eyes or mucous membranes ■ do not bandage tightly

📄 Stop Use and Ask a Doctor If 59 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 ■ when using for pain of arthritis if: ■ pain persists for more than 10 days ■ redness is present ■ in conditions affecting children under 12 years of age

📄 Keep Out of Reach of Children 23 words ▾

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

📄 Questions or Comments 23 words ▾

Questions or comments? (888) 221-3496 M-F 9 am to 5 pm ■ you may also report serious side effects to this phone number

📄 Package Label / Principal Display Panel 65 words ▾

WU YANG BRAND PAIN RELIEVING MEDICATED PLASTER External Analgesic NDC 55614-700-01 Large Pain Relief Patches 10 Plasters Each plaster 3.9 x 11 inches (10 x 28 cm) - 1 Plaster per pouch IMAGE OF BOX

WU YANG BRAND PAIN RELIEVING MEDICATED PLASTER External Analgesic NDC 55614-700-02 Cut To Size Pain Relief Patches 1 Plaster 3.9 x 78.7 inches (10 x 200 cm) IMAGE OF CANISTER

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 MENTHOL AND CAMPHOR — the ingredient across all brands.

Top reported reactions

Illness1
Influenza Like Illness1
Lethargy1
Vomiting1

Reporter sex

2 reports
Female · 100%
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 1 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 MADISON ONE ACME INC. 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 1 patch (55614-0700-02). 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?
MADISON ONE ACME INC 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.
← 55614-0690-01 · MADISON 55614-0711-01 · MADISON →
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.