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Traditional Chinese Medicine Health Card and TCM Epidemic Prevention Card Natural Herbal Antibacterial Card and TCM Magic .5 g/6.5g; 1 g/6.5g; 1 g/6.5g Powder, 6.5 g — NDC 81831-0101-01 package photo

Traditional Chinese Medicine Health Card and TCM Epidemic Prevention Card Natural Herbal Antibacterial Card and TCM Magic .5 g/6.5g; 1 g/6.5g; 1 g/6.5g Powder, 6.5 g

by Chuanzongbao (Hangzhou) intangible cultural heritage protection Co., Ltd · 6.5 g in 1 BOX (81831-101-01)
NDC 81831-0101-01
🏷️ FDA NDC (as labeled) 81831-101-01 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Inactivated by FDA
🗂️ Data synced 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

⚠️
Excluded from the active FDA NDC Directory. FDA inactivated this product’s listing record, so it is excluded from the active NDC Directory. The listing was last certified through Dec 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 81831-101-01
Product NDC 81831-101
11-digit billing NDC 81831010101
UNII M89NIB437X, FV98Z8GITP, 1V63N2S972
UPC 6973375960016
SPL Set ID c00de1a5-8713-2200-e053-2a95a90a7e9a
DEA schedule Non-controlled
Marketing category UNAPPROVED DRUG OTHER
Marketing status Discontinued
FDA listing status Inactivated by FDA (certified through Dec 2026)
Marketing start 2021-04-16
Route TOPICAL
Dosage form POWDER
Substance BORNEOL; MINT; ANGELICA DAHURICA ROOT
Why two NDCs? The FDA registers this code as 81831-101-01 — 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 → 81831-0101-01. 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

LabelerChuanzongbao (Hangzhou) intangible cultural heritage protection Co., Ltd
Labeler code81831
First marketedApr 2021
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.

🩺 Clinical

🧪 What is this product?

This is an unapproved topical powder product containing angelica dahurica root, borneol, and mint. It is marketed as a traditional Chinese medicine product intended for antibacterial and epidemic prevention purposes. Angelica dahurica root and mint are herbs commonly used in traditional medicine formulations, while borneol is a compound derived from plant sources that is typically included in topical preparations for its aromatic and cooling properties. This product has not undergone FDA approval review.

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 4899NQQ8FK
    A plant extract from sweet flag grass used in traditional herbal formulations. It may act as a flavoring agent, preservative, or texture modifier in medicines and supplements.
  • UNII U4KXI7P9Z1
    A plant extract from agastache rugosa, an aromatic herb. It may serve as a flavoring agent, fragrance, or natural additive to enhance taste or aroma in the medicine.
  • 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 CAZ6282J2O
    Atractylodes lancea root is a plant-derived ingredient used in traditional Asian medicine formulations. It typically serves as a filler or supporting agent to add bulk and help bind other ingredients in the medicine.
  • UNII 3EMP8C3I0X
    A plant-derived ingredient from the Cyperus rotundus (nutgrass) plant. It's used in formulations as a natural filler and binding agent to help hold the tablet or capsule together and maintain product stability.
  • UNII RR83T99U97
    A plant-derived substance from Asian lovage root used in traditional formulations. It may serve as a flavoring agent, fragrance component, or natural additive to support product stability and palatability.
  • UNII 8LCB7ZW9UL
    A plant extract from magnolia flower blossoms. It may serve as a flavoring agent, fragrance, or natural colorant in the medicine to improve taste, smell, or appearance.

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

The official label also statesARTEMISIA PRINCEPS LEAF ACORUS CALAMUS VAR. ANGUSTATUS WHOLE MAGNOLIA ACUMINATA FLOWER AGASTACHE RUGOSA WHOLE CYPERUS ROTUNDUS WHOLE ATRACTYLODES LANCEA ROOT LIGUSTICUM SINENSE SUBSP. CHUANXIONG 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.

💲 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 gPer 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Traditional Chinese Medicine Health Card and TCM Epidemic Prevention Card .5 g/6.5g; 1 g/6.5g; 1 g/6.5gthis 81831-0101-01 Chuanzongbao 6.5 g — — Discontinued —
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

🏛️
2021
On the market since
Apr 2021
📍
2026
Currently FDA-listed
5 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
81831-0101-01 You're viewing this 6.5 g in 1 BOX (81831-101-01) 2021-04-16 Inactivated by FDA

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Marketed without an FDA application No longer marketed (per FDA listing data)

Listed without an FDA application

This product's marketing category indicates it is marketed without an approved FDA application (no NDA, ANDA, or BLA on file). Having an NDC does not by itself establish FDA approval — the NDC Directory is a listing system, not an approval decision. Approval-linked data such as Orange Book therapeutic-equivalence ratings therefore does not apply.

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 "Unapproved Drug Other". 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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 81831-101-01, 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: 81831-0101-01, written without dashes as 81831010101. 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 81831-0101-01, the first segment (81831) is the labeler code FDA assigned to Chuanzongbao (Hangzhou) intangible cultural heritage protection Co., Ltd; the middle segment (0101) 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.
Who lists this product with the FDA?
Chuanzongbao (Hangzhou) intangible cultural heritage protection 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 19 words ▾

Use For wearing on the body, Full scene, through herbal aromatherapy, refreshing energy, enhancing virus resistance, and enhancing immunity

⏱️ Dosage and Administration 52 words ▾

Directions Wear it on your chest like a work permit or put it in your jacket pocket to receive aromatherapy for every day. Sniffing for 2-3 minutes a day can regulate qi and expectorant, improve refreshment, and reduce bacterial infections Continuous long-term wearing, receiving Chinese medicine aromatherapy conditioning, can improve human immunity

⚠️ Warnings 5 words ▾

Warnings For external use only.

📦 Storage and Handling 11 words ▾

Other information Store in a cool dry place below 104 ℃F

🧪 Active Ingredient 10 words ▾

Active Ingredient(s) ANGELICA DAHURICA ROOT 0.5g/6.5g MINT 1g/6.5g BORNEOL 1g/6.5g

🧪 Inactive Ingredients 27 words ▾

Inactive ingredients ARTEMISIA PRINCEPS LEAF ACORUS CALAMUS VAR. ANGUSTATUS WHOLE MAGNOLIA ACUMINATA FLOWER AGASTACHE RUGOSA WHOLE CYPERUS ROTUNDUS WHOLE ATRACTYLODES LANCEA ROOT LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT

🎯 Purpose 5 words ▾

Purpose Antibacterial and Health Care

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 81826-0001-01 · CODAN 81839-0782-02 · CSL →
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.