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YULAM DIE DA WAN HUA PAIN RELIEVING Menthol and Camphor 3 g/100mL; 4 g/100mL Oil — NDC 55614-0740-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

YULAM DIE DA WAN HUA PAIN RELIEVING Menthol and Camphor 3 g/100mL; 4 g/100mL Oil — NDC 55614-740-01 (Billing 55614-0740-01)

by MADISON ONE ACME INC · 1 BOTTLE, PLASTIC in 1 BOX / 50 mL in 1 BOTTLE, PLASTIC

This is a package of YULAM DIE DA WAN HUA PAIN RELIEVING Menthol and Camphor 3 g/100mL; 4 g/100mL Oil from MADISON ONE ACME INC, marketed since Jun 2023 and currently FDA-listed, this package's marketing is listed to end Jun 2027. It is this product's only package size.

NDC 55614-0740-01
🏷️ FDA NDC (as labeled) 55614-740-01 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 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 55614-740-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
55614 labeler · 740 product · 01 package
Package marketed since
Jun 1, 2023
Package marketing ended
Jun 1, 2027
Sample package
No — commercial package
Barcode (UPC-A, from the NDC)
3 5561474001 0
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 55614-740-01
Product NDC 55614-740
11-digit billing NDC 55614074001
RxCUI 2619676
UNII L7T10EIP3A, 5TJD82A1ET
Application # M017
SPL Set ID 1ba3c31b-2737-4b55-a0ea-90013a1d8cf4
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-06-01
Marketing end 2027-06-01
Route TOPICAL
Dosage form OIL
Substance MENTHOL; CAMPHOR (SYNTHETIC)
Quick answers
  • RxCUI (RxNorm): 2619676
Why two NDCs? The FDA registers this code as 55614-740-01 — 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 → 55614-0740-01. 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?

Yulam Die Da Wan Hua Pain Relieving is a topical oil product containing menthol and camphor. This is an over-the-counter monograph drug, meaning it is marketed under FDA's established category rules for topical pain-relief products. Menthol and camphor are commonly used in topical preparations for their cooling and warming sensations, which are typically intended to provide temporary comfort to muscles and joints 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
55614-0740-01 You're viewing this Main listing 1 BOTTLE, PLASTIC in 1 BOX / 50 mL in 1 BOTTLE, PLASTIC 2022-11-02 Jun 1, 2027 Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Yulam Die Da Wan Hua Pain Relieving 3 g/100mL; 4 g/100mLthis 55614-0740-01 MADISON 1 bottle — — 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
Jun 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 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 0MF1EI01KJ
    Angelica pubescens root is a plant-derived ingredient used as a flavoring agent and traditional botanical component in some herbal and natural formulations to enhance taste and provide characteristic aroma.
  • UNII T1PE06G0VE
    Camellia oil is a plant-based oil extracted from camellia seeds. It's used in medicines as an emollient and lubricant to improve texture and help ingredients blend smoothly together.
  • 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 5Y143KS0YL
    A plant extract from wintersweet flowers used in traditional formulations. It may function as a botanical ingredient to enhance flavor, aroma, or provide natural coloring in the medicine.
  • UNII I6OER6U04L
    A plant extract from chrysanthemum flowers used as a natural colorant and flavoring agent in medicines. It may contribute mild taste or visual appeal to the final product.
  • UNII EW5ECF6XAX
    A plant extract from the roots of Curcuma involucrata, a relative of turmeric. It may be used as a natural colorant or flavoring agent in the medicine.
  • UNII CZP7EPR012
    A plant-derived ingredient from the root of Cynanchum paniculatum. It may function as a binder or thickening agent to help hold the medicine together or improve its consistency in the formulation.
  • 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 A6W0J6UO7Q
    A plant-derived extract from the fruit of the Chinese honey locust tree. It serves as a natural thickener and emulsifier to help blend ingredients and create a smooth, uniform texture in medicines.
  • UNII 32SLT970XO
    A plant extract from Chinese ligusticum root, traditionally used in herbal medicine. In pharmaceutical formulations, it may serve as an active botanical ingredient or flavor component, though its specific excipient role varies by product.
  • UNII 517Q7XRT2T
    A plant-derived ingredient from the root of Lindera aggregata. It may be used as a natural flavoring agent, fragrance component, or traditional botanical extract in formulations.
  • UNII J1BO4MHT2L
    A plant material from Canadian mint that provides flavor and aroma to the medicine. It's used to improve taste and make the product more pleasant to take.
  • UNII 5Z2WW4J6RI
    A plant root extract used in traditional herbal formulations. It may function as an active botanical ingredient or flavoring agent, though in many modern medicines it serves primarily to support the product's traditional composition and stability.
  • UNII BUG255FE7X
    A plant-derived ingredient from tree peony root bark. It's used in traditional formulations as a natural filler and may help stabilize the medicine's consistency and appearance.
  • UNII HAM6R1WA7O
    A plant extract from kudzu flowering tops used as a natural flavoring or coloring agent in medicines. It may help mask taste or add color to the final product.
  • UNII G025DAL7CE
    A plant extract from rhubarb root used as a natural colorant and flavoring agent in medicines. It may also help stimulate bowel movement in laxative formulations.
  • 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 46N107B71O
    Shellac is a natural resin secreted by the lac beetle. It's used as a coating on tablets and capsules to control how quickly the medicine dissolves and to improve appearance and stability.
  • UNII 7FA55IY5H8
    A plant-derived ingredient from flower buds of Syzygium nervosum. Used in formulations as a flavoring agent, colorant, or traditional botanical component to enhance taste or appearance.
  • UNII JU3D414057
    A natural plant extract from tangerine fruit peel used as a flavoring agent and color contributor. It adds tangerine taste and may provide a slight orange tint to medicines.
  • UNII B077C3NLJV
    A natural plant extract from unripe tangerine fruit peel, used as a flavor ingredient to add citrus taste and aroma to medicines.
  • UNII TN770YC17C
    A plant-derived ingredient from the Xanthium strumarium fruit. It's used in formulations as a natural binder and filler to help hold the medicine together and add bulk to tablets or capsules.
  • 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.

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

The official label also statesInactive ingredients angelica dahurica (bai zhi) root, angelica pubescens (du huo) root, camellia oil, carthamus tinctorius (hong hua) flower bud, chimonanthus praecox (la mei hua) flower, chrysanthemum indicum (yeh chu hua) flower, curcuma involucrata (tu tian qi) root, cynanchum paniculatum (xu chang pu) root, drynaria fortunei (gu sui bu) root, gardenia jasminoides (zhi zi) fruit, ginger (jiang) root, gleditsia sinensis (da zao jiao) fruit, pueraria montana var. lobata (ge hua) flower top, ligusticum sinense (chuan xiong) root, lindera aggergata (wu yao) root, mentha canadensis (bo he) oil, notopterygium incisum (qiang huo) root, paeonia x suffruticosa (mu dan pi) root bark, rheum palmatum (da huang) root, saposhnikovia divaricata (fang feng) root, shellac, syzygium nervosum flower bud, tangerine (qing pi) unripe peel, tangerine (chen pi) peel, xanthium strumarium (cang er zi) fruit, zanthoxylum nitidum (liang mian zhen) root.

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 marketedJun 2023
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 🤒 Adverse Reactions 📦 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: ■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains

⏱️ Dosage and Administration 41 words ▾

Directions ■ adults and children 2 years of age and older: Apply to affected area and rub gently. Do not use for more than 4 times a day. ■ children under 2 years of age: Do not use, consult a doctor.

⚠️ Warnings 5 words ▾

Warnings For external use only

🤒 Adverse Reactions 16 words ▾

Report any unexpected side effects from the use of this product to the FDA MedWatch Program.

📦 Storage and Handling 17 words ▾

Other information ■ keep container tightly closed ■ store in a cool dry place away from sunlight

🧪 Active Ingredient 6 words ▾

Active ingredient Menthol 3% Camphor 4%

🧪 Inactive Ingredients 136 words ▾

Inactive ingredients angelica dahurica (bai zhi) root, angelica pubescens (du huo) root, camellia oil, carthamus tinctorius (hong hua) flower bud, chimonanthus praecox (la mei hua) flower, chrysanthemum indicum (yeh chu hua) flower, curcuma involucrata (tu tian qi) root, cynanchum paniculatum (xu chang pu) root, drynaria fortunei (gu sui bu) root, gardenia jasminoides (zhi zi) fruit, ginger (jiang) root, gleditsia sinensis (da zao jiao) fruit, pueraria montana var. lobata (ge hua) flower top, ligusticum sinense (chuan xiong) root, lindera aggergata (wu yao) root, mentha canadensis (bo he) oil, notopterygium incisum (qiang huo) root, paeonia x suffruticosa (mu dan pi) root bark, rheum palmatum (da huang) root, saposhnikovia divaricata (fang feng) root, shellac, syzygium nervosum flower bud, tangerine (qing pi) unripe peel, tangerine (chen pi) peel, xanthium strumarium (cang er zi) fruit, zanthoxylum nitidum (liang mian zhen) root.

🎯 Purpose 5 words ▾

Purpose External analgesic External analgesic

📄 Do Not Use 12 words ▾

Do not use ■ on wounds ■ on irritated or damaged skin

📄 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 75 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 ■ excessive irritation of the skin develops ■ nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs ■ when using for pain of arthritis: ■ 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 20 words ▾

YULAM DIE DA WAN HUA PAIN RELIEVING OIL NDC 55614-740-01 EXTERNAL ANALGESIC

1.7 FL OZ (50 ML) IMAGE OF BOX

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 it is currently marketed — but MADISON ONE ACME INC has reported a marketing end date of 2027-06-01, after which this package is expected to stop being marketed. The directory data on this page refreshes weekly.
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.
← 55614-0730-01 · MADISON 55621-0001-01 · 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.