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TRIHERBAL Arnica montana, Phytolacca decandra, Sanguinaria canadensis 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1 Capsule, 120-count — NDC 71989-718-21 (Billing 71989-0718-21)

by Spaus Inc. · 1 BOTTLE in 1 BOX / 120 CAPSULE in 1 BOTTLE

This is a package of 120 capsules of TRIHERBAL Arnica montana, Phytolacca decandra, Sanguinaria canadensis 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1 Capsule from Spaus Inc., no longer marketed (first marketed Jan 2026), no longer in the FDA NDC Directory.

NDC 71989-0718-21
🏷️ FDA NDC (as labeled) 71989-718-21 billing pads the product segment with a zero
This package
Contains120-count Pack sizes3 compare ↓
Product page 71989-0718-20 Also comes in: 60 capsules 71989-718-20 180 capsules 71989-718-22
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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

NDC database record

One package, one record: these facts belong to NDC 71989-718-21 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
71989 labeler · 718 product · 21 package
Package marketed since
Jan 1, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 7198971821 8
FDA record last changed
Jul 24, 2026
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Sep 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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 71989-718-21
Product NDC 71989-718
11-digit billing NDC 71989071821
UNII O80TY208ZW, 11E6VI8VEG, N9288CD508
SPL Set ID 716e23f3-43eb-43e6-b6f9-2043c420f19e
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Sep 2026)
Marketing start 2026-01-01
Route ORAL
Dosage form CAPSULE
Substance ARNICA MONTANA WHOLE; PHYTOLACCA AMERICANA ROOT; SANGUINARIA CANADENSIS ROOT
Why two NDCs? The FDA registers this code as 71989-718-21 — 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 → 71989-0718-21. 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?

Triherbal is an unapproved homeopathic oral capsule containing arnica montana, phytolacca americana root, and sanguinaria canadensis root. In homeopathic practice, these plant materials are traditionally used to address minor swelling, inflammation, and skin concerns, though homeopathic products are not evaluated by the FDA for effectiveness. This product is marketed based on homeopathic tradition rather than clinical evidence.

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: 60 capsules 180 capsules
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
71989-0718-20 71989-718-20 Main listing 1 BOTTLE in 1 BOX / 60 CAPSULE in 1 BOTTLE 2026-01-01 — Discontinued by firm
71989-0718-21 You're viewing this 1 BOTTLE in 1 BOX / 120 CAPSULE in 1 BOTTLE 2026-01-01 — Discontinued by firm
71989-0718-22 71989-718-22 1 BOTTLE in 1 BOX / 180 CAPSULE in 1 BOTTLE 2026-01-01 — Discontinued by firm

Pack size FAQ

What quantity is in this package?
This is a 120-count package — 1 bottle in 1 box / 120 capsule in 1 bottle.
How does this package differ from NDC 71989-0718-20?
Both are TRIHERBAL Arnica montana, Phytolacca decandra, Sanguinaria canadensis 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1 Capsule — the drug itself is identical. This page's package is the 120-count one, while NDC 71989-0718-20 is the 60 capsules package.
What NDC number is used to bill for this package of TRIHERBAL Arnica montana, Phytolacca decandra, Sanguinaria canadensis 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1 Capsule?
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
Triherbal 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]this 71989-0718-21 Spaus 120 capsules — — 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

🏛️
2026
On the market since
Jan 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerSpaus Inc.
Labeler code71989
First marketedJan 2026
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 📄 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 33 words ▾

Uses Temporarily relieves minor aches, pains, and inflammation due to: ▪ Headache ▪ Menstrual cramps ▪ Minor pain of arthritis ▪ Backache ▪ Neuralgia ▪ Temporarily reduces fever ▪ Toothache ▪ Muscular aches

⏱️ Dosage and Administration 25 words ▾

Directions: Adults and children 12 years and older: Swallow 1-2 capsules every 4 – 6 hours as needed. Children under 12 years: Consult a doctor.

⚠️ Warnings 45 words ▾

Warnings Stop and ask a doctor if symptoms persist for more than 3 days or worsen. If pregnant or breastfeeding, ask a healthcare professional before use. Keep out of reach of children. In case of overdose, seek medical help or contact Poison Control Center immediately.

🧪 Active Ingredient 43 words ▾

Active Ingredients (in each capsule) Arnica montana 3X HPUS* (0.02%) Phytolacca decandra 3X HPUS* (0.02%) Sanguinaria canadensis 3X HPUS* (0.02%) HPUS indicates the active ingredients are officially monographed in the Homeopathic Pharmacopoeia of the United States. X is a homeopathic dilution, see www.triherbal.com

🧪 Inactive Ingredients 9 words ▾

Inactive Ingredients: ß-cyclodextrin, clove extract, hypromellose (capsule), turmeric extract.

🎯 Purpose 29 words ▾

Purpose: Homeopathic medicine Relieves Inflammation, swelling, menstrual cramps, muscle soreness, fever & joint, back, neck, tooth pain Relieves Inflammation, fever, stiffness, arthritis pain Relieves headache, migraine, sore throat, neuralgia

📄 Stop Use and Ask a Doctor If 15 words ▾

Stop and ask a doctor if symptoms persist for more than 3 days or worsen.

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant or breastfeeding, ask a healthcare professional before use.

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. In case of overdose, seek medical help or contact Poison Control Center immediately.

📄 Other Information 21 words ▾

Other Information ▪ store below 86°F (30°C) Dist. by: Haus Bioceuticals Inc. 755 Research Park, Ste. 461 Oklahoma City, OK 73104

📄 Questions or Comments 165 words ▾

Questions or Comments? – 60 Count Box Label TriHerbal.com [email protected] 1-405-708-4635 Do not use if seal under cap is broken or missing. *Claims based on traditional homeopathic practice, not accepted medical evidence. These statements have not been evaluated by the Food and Drug Administration. NDC: 71989-718-20 v: No NSAIDs No acetaminophen No know drug interactions

Questions or Comments? – 120 Count Box Label TriHerbal.com [email protected] 1-405-708-4635 Do not use if seal under cap is broken or missing. *Claims based on traditional homeopathic practice, not accepted medical evidence. These statements have not been evaluated by the Food and Drug Administration. NDC: 71989-718-21 v: No NSAIDs No acetaminophen No know drug interactions

Questions or Comments? – 180 Count Box Label TriHerbal.com [email protected] 1-405-708-4635 Do not use if seal under cap is broken or missing. *Claims based on traditional homeopathic practice, not accepted medical evidence. These statements have not been evaluated by the Food and Drug Administration. NDC: 71989-718-22 v: No NSAIDs No acetaminophen No know drug interactions

📄 Package Label / Principal Display Panel 57 words ▾

Package/Label Principal Display Panel – 60 Count Box Label TRIHERBAL™ NATURAL PAIN RELIEVER 60 Capsules, 600 mg each image-060

Package/Label Principal Display Panel – 120 Count Box Label TRIHERBAL™ NATURAL PAIN RELIEVER 120 Capsules, 600 mg each image-120

Package/Label Principal Display Panel – 180 Count Box Label TRIHERBAL™ NATURAL PAIN RELIEVER 180 Capsules, 600 mg each image-180

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 Homeopathic listing No longer marketed (per FDA listing data)

About homeopathic listings

TRIHERBAL Arnica montana, Phytolacca decandra, Sanguinaria canadensis 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1 CAPSULE is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 Homeopathic". 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 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.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 60 capsules (71989-0718-20), 180 capsules (71989-0718-22). 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?
Spaus 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.
← 71981-0020-07 · Domp 71990-0001-01 · Arcadia →
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.