Home › NDC Lookup › Ingredients › Peppermint, Camphor, Borneol › 85305-0004-01
BANPINGHUA Glucosamine Chondroitin Patch PEPPERMINT, CAMPHOR, BORNEOL .01 g; .01 g; .02 g Patch, 7 patches — NDC 85305-0004-01 package photo

BANPINGHUA Glucosamine Chondroitin Patch PEPPERMINT, CAMPHOR, BORNEOL .01 g; .01 g; .02 g Patch, 7 patches

by Henan Lijitang Medical Technology Co., Ltd. · 7 PATCH in 1 BAG (85305-004-01) / 1 PATCH in 1 PATCH
NDC 85305-0004-01
🏷️ FDA NDC (as labeled) 85305-004-01 billing pads the product segment with a zero
This package
Contains7 patches Pack sizes4 compare ↓
Also comes in: 10 patches 85305-0004-02 15 patches 85305-0004-03 30 patches 85305-0004-04
OTC On market Non-controlled
🗂️ Data synced 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

🆔 Identity & classification

FDA NDC (as labeled) 85305-004-01
Product NDC 85305-004
11-digit billing NDC 85305000401
UNII M89NIB437X, V95R5KMY2B, 32K0C7JGCJ
UPC 6978507461959
Application # M017
SPL Set ID 42f8c2ae-50a2-2358-e063-6394a90a5979
Established class (EPC) Non-Standardized Plant Allergenic Extract; Non-Standardized Food Allergenic Extract
Physiologic effect Increased Histamine Release; Cell-mediated Immunity
Chemical class Allergens; Dietary Proteins; Plant Proteins; Food Additives
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-11-07
Route TOPICAL
Dosage form PATCH
Substance BORNEOL; PEPPERMINT; CAMPHORIC ACID
Why two NDCs? The FDA registers this code as 85305-004-01 — 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 → 85305-0004-01. 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.

🏭 Manufacturer & labeler

LabelerHenan Lijitang Medical Technology Co., Ltd.
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code85305
First marketedNov 2025
Product typeHuman Otc Drug
Portfolio4 products on file
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.

🩺 Clinical

🧪 What is this product?

This is a topical patch containing peppermint, camphor, and borneol as active ingredients. These substances are commonly used in over-the-counter topical products for their warming and cooling sensations, which are typically intended to provide localized comfort. The patch is marketed as an OTC monograph drug, meaning it follows FDA's established rules for this category of product rather than being individually reviewed. This product is applied directly 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.

🧪 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 SY077EW02G
    A plant extract from Artemisia princeps (mugwort) leaves used in some formulations as a flavoring agent, fragrance component, or traditional ingredient. It may also serve minor roles in product stability or sensory appeal.
  • UNII WS4CQ062KM
    A plant-derived spice from cinnamon bark, used as a flavoring agent to mask bitter tastes and add pleasant aroma to medicines.
  • 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 750W5330FY
    Glucosamine hydrochloride is an amino sugar derived from shellfish or produced synthetically. In medicines, it serves as an active nutritional ingredient rather than a typical inactive excipient, used to support joint and cartilage function.
  • UNII N1Y8OM2BQ7
    Kadsura coccinea root is a plant-derived ingredient used as a natural flavoring or taste-masking agent in medicines. It helps improve the palatability of formulations, particularly in liquid or chewable products.
  • UNII 1F3X9DRV9X
    Laurocapram is a synthetic oily liquid used as a penetration enhancer and solvent in topical medicines. It helps active ingredients absorb better through the skin and improves how the medication spreads across the application area.
  • UNII CI148ZPI0D
    A fine powder derived from clubmoss spores, used as a glidant and anti-caking agent to improve powder flow and prevent clumping in solid medications.
  • UNII 6G287VJM69
    A plant-derived ingredient from Phryma leptostachya (lopseed plant). It serves as a natural filler or binder to help hold the medicine's ingredients together in solid form.
  • UNII H5BJH23Z9A
    A natural polymer extracted from porcine (pig) cartilage tissue. It acts as a binder to hold tablet ingredients together and may improve the product's texture and consistency during manufacturing.
  • UNII 9DE5YCO0RU
    A plant extract from dandelion root traditionally used in herbal preparations. In medications, it may serve as a flavor enhancer, natural colorant, or bitter component that supports formulation taste and appearance.
  • UNII 856YO1Z64F
    Turmeric is a natural spice derived from the turmeric plant root. It serves as a colorant in medicines, giving products a yellow or golden appearance, and may also provide mild flavoring.

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

The official label also statesDANDELION EXTRACT, MUGWORT EXTRACT, TURMERIC EXTRACT, CINNAMON EXTRACTCYNANCHUM PANICULATUM. LYCOPODIUM CLAVATUM, PHRYMA LEPTOSTACHYA, GLUCOSAMINEHYDROCHLORIDE, SODIUM CHONDROITIN SULFATE, KADSURA HETEROCLITA STEM, AZONE

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.

💲 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: 10 patches 15 patches 30 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
BANPINGHUA Glucosamine Chondroitin Patch .01 g/1; .01 g/1; .02 gthis 85305-0004-01 Henan 7 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

🏛️
2025
On the market since
Nov 2025
📍
2026
Currently FDA-listed
1 year 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
85305-0004-01 You're viewing this 7 PATCH in 1 BAG (85305-004-01) / 1 PATCH in 1 PATCH 2025-11-07 Active
85305-0004-02 10 PATCH in 1 BAG (85305-004-02) / 1 PATCH in 1 PATCH 2025-11-07 Active
85305-0004-03 15 PATCH in 1 BAG (85305-004-03) / 1 PATCH in 1 PATCH 2025-11-07 Active
85305-0004-04 30 PATCH in 1 BAG (85305-004-04) / 1 PATCH in 1 PATCH 2025-11-07 Active

Pack size FAQ

What quantity is in NDC 85305-0004-01?
NDC 85305-0004-01 contains 7 patches — 7 patch in 1 bag / 1 patch in 1 patch.
What is the difference between NDC 85305-0004-01 and NDC 85305-0004-02?
Both are BANPINGHUA Glucosamine Chondroitin Patch PEPPERMINT, CAMPHOR, BORNEOL .01 g; .01 g; .02 g Patch — the drug itself is identical. NDC 85305-0004-01 is the 7 patches package, while NDC 85305-0004-02 is the 10 patches package.
What NDC number is used to bill for this package of BANPINGHUA Glucosamine Chondroitin Patch PEPPERMINT, CAMPHOR, BORNEOL .01 g; .01 g; .02 g Patch?
Bill NDC 85305-0004-01 — the 11-digit billing format is 85305000401. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 FDA registers it as 85305-004-01, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 85305-0004-01, written without dashes as 85305000401. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 85305-0004-01, the first segment (85305) is the labeler code FDA assigned to Henan Lijitang Medical Technology Co., Ltd.; the middle segment (0004) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
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 Henan Lijitang Medical 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 3 other package presentations of this same product, including 10 patches (85305-0004-02), 15 patches (85305-0004-03), 30 patches (85305-0004-04). 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?
Henan Lijitang Medical 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.

📄 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
🎯 Indications and Usage 31 words ▾

Suitable For: Individuals who are experiencing discomfort, pain, or numbness in various joint areas. It has a health effect of relieving and requlating discomfort, joint pain, numbness, etc. in various joints.

⏱️ Dosage and Administration 26 words ▾

Directions for Use: Remove the transparent film and apply the patch to the desiredarea or corresponding acupuncture point. Each patch may be worn for 8-12 hours.

⚠️ Warnings 9 words ▾

This product is intended for single-use external application only.

🧪 Active Ingredient 6 words ▾

PEPPERMINT 1% CAMPHOR 2% BORNEOL 1%

🧪 Inactive Ingredients 21 words ▾

DANDELION EXTRACT, MUGWORT EXTRACT, TURMERIC EXTRACT, CINNAMON EXTRACTCYNANCHUM PANICULATUM. LYCOPODIUM CLAVATUM, PHRYMA LEPTOSTACHYA, GLUCOSAMINEHYDROCHLORIDE, SODIUM CHONDROITIN SULFATE, KADSURA HETEROCLITA STEM, AZONE

🎯 Purpose 1 words ▾

Analgesia

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85305-0003-01 · Henan 85306-0204-21 · INTEGRATIVE →
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.