![TRIHERBAL Arnica montana, Phytolacca decandra, Sanguinaria canadensis 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1 Capsule, 180-count — NDC 71989-0718-22 package photo](https://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=716e23f3-43eb-43e6-b6f9-2043c420f19e&name=image-060.jpg)
TRIHERBAL Arnica montana, Phytolacca decandra, Sanguinaria canadensis 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1 Capsule, 180-count
by Spaus Inc. · 1 BOTTLE in 1 BOX (71989-718-22) / 180 CAPSULE in 1 BOTTLE
NDC 71989-0718-22
🏷️ FDA NDC (as labeled)
71989-718-22
billing pads the product segment with a zero
This package
Contains180-count
Pack sizes3 compare ↓
OTC
On market
Non-controlled
🗂️ 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 →
🆔 Identity & classification
FDA NDC (as labeled)
71989-718-22
Product NDC
71989-718
11-digit billing NDC
71989071822
UNII
O80TY208ZW, 11E6VI8VEG, N9288CD508
SPL Set ID
716e23f3-43eb-43e6-b6f9-2043c420f19e
DEA schedule
Non-controlled
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing status
On market
FDA listing status
Listed (active directory)
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 71989-718-22 — 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 → 71989-0718-22. 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
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.
🩺 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.
Patient education
Supplement & herbal interactions
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.
💬 Questions about Arnica montana, Phytolacca decandra, Sanguinaria canadensis?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
Orange
ShapeCapsule
Size23 mm
ScoringNot scored
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.
🧪 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 JV039JZZ3A
Betadex is a modified sugar molecule derived from starch. It acts as a solubilizer and stabilizer in medicines, helping dissolve poorly soluble drugs and keep them stable during storage.
-
UNII K48IKT5321
A plant extract from clove buds used as a flavoring agent and natural fragrance in medications. It adds taste and aroma to improve how the medicine smells and tastes.
-
UNII 3NXW29V3WO
Hypromellose is a plant-based thickener made from cellulose. It's used in medicines as a binder to hold ingredients together, a coating for tablets, and a thickener for liquids.
-
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.
4 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesß-cyclodextrin, clove extract, hypromellose (capsule), turmeric extract.
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 system | Per each | Per 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
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Triherbal 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]this 71989-0718-22 | Spaus | 180 capsules | — | — | 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
🏛️
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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 71989-0718-20 | 1 BOTTLE in 1 BOX (71989-718-20) / 60 CAPSULE in 1 BOTTLE | 2026-01-01 | Active |
| 71989-0718-21 | 1 BOTTLE in 1 BOX (71989-718-21) / 120 CAPSULE in 1 BOTTLE | 2026-01-01 | Active |
| 71989-0718-22 You're viewing this | 1 BOTTLE in 1 BOX (71989-718-22) / 180 CAPSULE in 1 BOTTLE | 2026-01-01 | Active |
Pack size FAQ
What quantity is in NDC 71989-0718-22?
NDC 71989-0718-22 is a 180-count package — 1 bottle in 1 box / 180 capsule in 1 bottle.
What is the difference between NDC 71989-0718-22 and 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. NDC 71989-0718-22 is the 180-count package, 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?
Bill NDC 71989-0718-22 — the 11-digit billing format is 71989071822. 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
Homeopathic listing
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 | ✓ 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 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.
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 71989-718-22, 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: 71989-0718-22, written without dashes as 71989071822. 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 71989-0718-22, the first segment (71989) is the labeler code FDA assigned to Spaus Inc.; the middle segment (0718) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (22) 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 Spaus 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 2 other package presentations of this same product, including 60 capsules (71989-0718-20), 120 capsules (71989-0718-21). 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.
📄 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 ▾
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 ▾
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 ▾
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 ▾
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 ▾
Inactive Ingredients: ß-cyclodextrin, clove extract, hypromellose (capsule), turmeric extract.
🎯 Purpose ▾
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
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.