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Traulevium Belladonna, Arnica Montana Radix, Aconitum Napellus, Chamomilla, Symphytum Officinale, Calendula Officinalis, Hamamelis Virginiana, Millefolium, Hepar Sulphuris Calcareum, Mercurius Solubilis, Hypericum Perforatum, Bellis Perennis, Echinacea Angustifolia, 4 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1; 8 [hp_X]/1; 2 [hp_X]/1; 2 [hp_X]/1 Tablet, Chewable, 100-count — NDC 70857-0002-10 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Traulevium Belladonna, Arnica Montana Radix, Aconitum Napellus, Chamomilla, Symphytum Officinale, Calendula Officinalis, Hamamelis Virginiana, Millefolium, Hepar Sulphuris Calcareum, Mercurius Solubilis, Hypericum Perforatum, Bellis Perennis, Echinacea Angustifolia, 4 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1; 8 [hp_X]/1; 2 [hp_X]/1; 2 [hp_X]/1 Tablet, Chewable, 100-count — NDC 70857-002-10 (Billing 70857-0002-10)

by Medical Technology Products, Inc. · 100 TABLET, CHEWABLE in 1 BOTTLE

This is a package of 100 tablets of Traulevium Belladonna, Arnica Montana Radix, Aconitum Napellus, Chamomilla, Symphytum Officinale, Calendula Officinalis, Hamamelis Virginiana, Millefolium, Hepar Sulphuris Calcareum, Mercurius Solubilis, Hypericum Perforatum, Bellis Perennis, Echinacea Angustifolia, 4 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1; 8 [hp_X]/1; 2 [hp_X]/1; 2 [hp_X]/1 Tablet, Chewable from Medical Technology Products, Inc., marketed since Oct 2016 and currently FDA-listed. It is this product's only package size.

NDC 70857-0002-10
🏷️ FDA NDC (as labeled) 70857-002-10 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 Oct 1, 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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 70857-002-10
Product NDC 70857-002
11-digit billing NDC 70857000210
UNII WQZ3G9PF0H, O80TY208ZW, U0NQ8555JD, G0R4UBI2ZZ, M9VVZ08EKQ, 18E7415PXQ +8 more
UPC 0742574246544
SPL Set ID 6123d145-4edf-4ecd-8b30-196e52273127
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2016-10-03
Route ORAL
Dosage form TABLET, CHEWABLE
Substance ATROPA BELLADONNA; ARNICA MONTANA; ACONITUM NAPELLUS; MATRICARIA RECUTITA; COMFREY ROOT; CALENDULA OFFICINALIS FLOWERING TOP; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; ACHILLEA MILLEFOLIUM; CALCIUM SULFIDE; MERCURIUS SOLUBILIS; HYPERICUM PERFORATUM; BELLI
Why two NDCs? The FDA registers this code as 70857-002-10 — 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 → 70857-0002-10. 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?

This is a chewable tablet containing multiple plant and mineral ingredients prepared according to homeopathic principles. The formula includes arnica, belladonna, aconitum, chamomilla, comfrey, calendula, witch hazel, yarrow, hepar sulphuris, mercury, St. John's wort, daisy, and echinacea at various homeopathic potencies. In homeopathic practice, these ingredients are traditionally used to address minor injuries, bruising, soreness, and wound healing, though homeopathic products are marketed based on traditional use and are not evaluated by the FDA for safety or effectiveness.

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
70857-0002-10 You're viewing this Main listing 100 TABLET, CHEWABLE in 1 BOTTLE 2016-10-03 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Traulevium 4 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1; 8 [hp_X]/1; 2 [hp_X]/1; 2 [hp_X]this 70857-0002-10 Medical 100 tablets — — 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

🏛️
2016
On the market since
Oct 2016
📍
2026
Currently FDA-listed
10 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.

What it looks like

Color white
ShapeRound
Imprint;
Size1 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 J2B2A4N98G
    Lactose is a natural sugar derived from milk. In medications, it serves as a filler and binder to add bulk and help hold tablet or capsule ingredients together during manufacturing.
  • UNII 70097M6I30
    Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.

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

The official label also statesInactive ingredients Lactose, Magnesium stearate.

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

LabelerMedical Technology Products, Inc.
Labeler code70857
First marketedOct 2016
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.

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 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 12 words ▾

Uses** For the temporary relief of: Joint Pain Back Pain Muscular Pain

⏱️ Dosage and Administration 126 words ▾

Directions Allow tablets to dissolve completely in the mouth, do not swallow. Standard Dosage Adults and children 12 years & older 3 tablets per day, taking 1 tablet every 4 to 6 hours. Children 4 to 11 years 2 tablets per day, taking 1 tablet every 6 to 8 hours.

Children under 4 years Consult your healthcare provider. Initial Dosage Adults and children 12 years & older 1 tablet every 1/2 to 1 hour, until symptoms lessen, then continue with standard dosage. Do not exceed 12 tablets in 24 hours.

Children 4 to 11 years 1 tablet every 1/2 to 1 hour, until symptoms lessen, then continue with standard dosage. Do not exceed 8 tablets in 24 hours. Children under 4 years Consult your healthcare provider.

⚠️ Warnings 71 words ▾

Warnings If symptoms worsen or persist for more than a week, a healthcare provider should be consulted. Do not use if known sensitivity to Traulevium or any of its ingredients exists. Keep out of the reach of children . In case of overdose, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding , ask a healthcare provider before use. Keep out of reach of children.

🧪 Active Ingredient 78 words ▾

Active ingredients (HPUS*) Each tablet contains as active ingredients: Belladonna 4X 75 mg, Arnica Montana Radix 3X 40 mg, Aconitum Napellus 3X 30 mg, Chamomilla 3X 24 mg, Symphytum Officinale 8X 24 mg, Calendula Officinalis 2X 15 mg, Hamamelis Virginiana 2X 15 mg, Millefolium 3X 15 mg, Hepar Sulphuris Calcareum 8X 15 mg, Mercurius Solubilis 8X 15 mg, Hypericum Perforatum 3X 8 mg, Bellis Perennis 2X 6 mg, Echinacea Angustifolia 2X 6 mg, Echinacea Purpurea 2X 6 mg.

🧪 Inactive Ingredients 5 words ▾

Inactive ingredients Lactose, Magnesium stearate.

🎯 Purpose 8 words ▾

Purpose** Relieves joint pain, back pain, muscular pain.

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children.

📄 Other Information 71 words ▾

Other information Tamper evident : Use this product only if imprinted shrink seal around the neck and cap is intact. Store tightly closed at room temperature. Protect from light and moisture. **These statements have not been reviewed by the Food and Drug Administration.

They are supported by traditional homeopathic principles. *The letters 'HPUS' indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States.

📄 Questions or Comments 31 words ▾

Questions? Call 1.866.440.7703 or email [email protected] Made in the USA. Manufactured exclusively for Medical Technology Products, Inc. by OHM pharma Inc. Medical Technology Products, Inc. Riviera Beach, FL 33407, USA. www.traulevium.com

📄 Package Label / Principal Display Panel 38 words ▾

NDC 70857-002-10 MTP Traulevium™ PAIN RELIEF TABLETS Homeopathic Medicine Compare to Traumeel®. Traumeel is a brand name owned by Biologische Heilmittel Heel GmbH. Traulevium is not associated with the brand owner. 100 Chewable Tablets 100 tablets bottle label

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

About homeopathic listings

Traulevium Belladonna, Arnica Montana Radix, Aconitum Napellus, Chamomilla, Symphytum Officinale, Calendula Officinalis, Hamamelis Virginiana, Millefolium, Hepar Sulphuris Calcareum, Mercurius Solubilis, Hypericum Perforatum, Bellis Perennis, Echinacea Angustifolia, 4 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1; 3 [hp_X]/1; 8 [hp_X]/1; 2 [hp_X]/1; 2 [hp_X]/1 TABLET, CHEWABLE 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 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: this package is listed as actively marketed, with no marketing end date reported by Medical Technology Products, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Medical Technology Products, 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.
← 70857-0001-50 · Medical 70857-0003-02 · Medical →
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.