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Arnicare Procedure Recovery ARNICA MONTANA Kit — NDC 00220-9050-75 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Arnicare Procedure Recovery ARNICA MONTANA Kit — NDC 0220-9050-75 (Billing 00220-9050-75)

by Laboratoires Boiron · 1 KIT in 1 PACKAGE * 80 PELLET in 1 TUBE

This is a package of Arnicare Procedure Recovery ARNICA MONTANA Kit from Laboratoires Boiron, marketed since Nov 2007 and currently FDA-listed. It is this product's only package size.

NDC 00220-9050-75
🏷️ FDA NDC (as labeled) 0220-9050-75 billing pads the labeler segment with a zero
OTC On market Non-controlled ⇄ 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 0220-9050-75 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
0220 labeler · 9050 product · 75 package
Package marketed since
Nov 1, 2007
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0306962827243
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 0220-9050-75
Product NDC 0220-9050
11-digit billing NDC 00220905075
UPC 0306962827243
SPL Set ID f0003627-b81c-46b6-8773-4f2987b75739
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2007-11-01
Route ORAL
Dosage form KIT
Why two NDCs? The FDA registers this code as 0220-9050-75 — a 4-4-2 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 labeler segment → 00220-9050-75. 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?

Arnicare Procedure Recovery is an unapproved homeopathic kit taken by mouth. Its active ingredient is Arnica Montana, a plant traditionally used in homeopathic practice. Homeopathic products are marketed on the basis of homeopathic tradition and theories, not on scientific evidence evaluated by the FDA. This product is not reviewed or approved 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
00220-9050-75 You're viewing this Main listing 1 KIT in 1 PACKAGE * 80 PELLET in 1 TUBE 2007-11-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Arnica Montana 3 [hp_X] 15631-0049-00 Rxhomeo 100 pellets — — FDA listed —
Arnica Montana 6 [hp_C] 63545-0159-01 Hahnemann 200 pellets — — FDA listed —
Arnica Montana 12 [hp_C] 63545-0160-01 Hahnemann 200 pellets — — FDA listed —
Arnica Montana 30 [hp_C] 63545-0161-01 Hahnemann 80 pellets — — FDA listed —
Arnica Montana 100 [hp_C] 63545-0162-01 Hahnemann 200 pellets — — FDA listed —
Arnica Montana 200 [hp_C] 63545-0163-01 Hahnemann 200 pellets — — FDA listed —
Arnica Montana 500 [hp_C] 63545-0164-01 Hahnemann 200 pellets — — FDA listed —
Arnica Montana 1 [hp_M] 63545-0165-01 Hahnemann 200 pellets — — FDA listed —
Arnica Montana 10 [hp_M] 63545-0166-01 Hahnemann 200 pellets — — FDA listed —
Arnica Montana 1 [hp_Q] 63545-0167-01 Hahnemann 10000 pellets — — FDA listed —
Arnica Montana 6 [hp_C]/6[hp_C] 66096-0789-01 OHM 1 tube — — FDA listed —
Arnica montana 5 [hp_C]/5[hp_C] 00220-0489-41 Boiron 1 tube — — FDA listed —
Arnica montana 200 [kp_C]/200[kp_C] 00220-0502-41 Boiron 1 tube — — FDA listed —
Arnica montana 10 [hp_M]/10[hp_M] 00220-0514-41 Boiron 1 tube — — FDA listed —
Arnica 30 [hp_C] 00220-0508-41 Laboratoires 80 pellets — — FDA listed —
Arnica montana 6 [hp_X]/6[hp_X] 00220-0519-41 Boiron 1 tube — — FDA listed —
Arnica montana 8 [hp_C]/8[hp_C] 00220-0493-41 Boiron 1 tube — — FDA listed —
Arnica montana 15 [hp_C]/15[hp_C] 00220-0501-41 Boiron 1 tube — — FDA listed —
Arnica montana 1 [hp_M]/[hp_M] 00220-0505-41 Boiron 1 tube — — FDA listed —
Arnica montana 30X Bonus Pack 30 [hp_X] 00220-9053-43 Boiron 3 tubes — — FDA listed —
BM Arnica Montana 30C 30 [hp_C]/1000mg 85816-5014-01 BM 30000 mg — — FDA listed —
Arnica Montana 6 [hp_C] 34666-0091-50 NARTEX 150 pellets — — FDA listed —
Arnica montana 200 [hp_X]/200[hp_X] 00220-0453-41 Boiron 1 tube — — FDA listed —
Arnica montana 3 [hp_C]/3[hp_C] 00220-0486-41 Boiron 1 tube — — FDA listed —
Arnica montana 30 [hp_X]/30[hp_X] 00220-0450-41 Boiron 1 tube — — FDA listed —
Arnica montana 3 [hp_X]/3[hp_X] 00220-0515-41 Boiron 1 tube — — FDA listed —
Arnicare Procedure Recoverythis 00220-9050-75 Laboratoires 1 kit — — FDA listed —
Arnica montana 12 [hp_X]/12[hp_X] 00220-0449-41 Boiron 1 tube — — FDA listed —
Arnica montana 6 [hp_C]/6[hp_C] 00220-0490-41 Boiron 1 tube — — FDA listed —
Arnica montana 12 [hp_C]/12[hp_C] 00220-0498-41 Boiron 1 tube — — FDA listed —
BM Arnica Mont 200 [hp_C]/g 85816-5015-01 BM 30 g — — FDA listed —
Arnica montana 9 [hp_C]/9[hp_C] 00220-0497-41 Boiron 1 tube — — FDA listed —
Bmnp Arnica Montana 30 [hp_C]/g 82969-5234-01 Total 25 g — — 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

🏛️
2007
On the market since
Nov 2007
📍
2026
Currently FDA-listed
19 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;
Size4 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.

From the label’s inactive-ingredient sectionlactose, sucrose

This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.

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

LabelerLaboratoires Boiron
Labeler code00220
First marketedNov 2007
Product typeHuman Otc Drug
Portfolio40 products on file

More NDCs from Laboratoires Boiron labeler code 00220

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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Ask a Doctor Before Use If 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 25 words ▾

Uses* temporarily relieves minor muscle pain and stiffness due to: minor injuries overexertion falls minor procedures reduces symptoms of bruising such as: pain swelling discoloration

⏱️ Dosage and Administration 32 words ▾

Directions Before procedure: Dissolve 5 pellets under the tongue 3 times a day for 2 days. After procedure: Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved.

🧪 Active Ingredient 32 words ▾

Active ingredient** (in each pellet) Arnica montana 12C (0.44 mg) HPUS The letters "HPUS" indicate that the component in this product is officially monographed in the Homeopathic Pharmacopoeia of the United States.

🧪 Inactive Ingredients 2 words ▾

lactose, sucrose

🎯 Purpose 13 words ▾

Purpose* Relieves minor muscle pain & stiffness, swelling from injuries, discoloration from bruises

📄 Ask a Doctor Before Use If 27 words ▾

Ask a doctor before use if pain, stiffness or bruising limits the range of motion of your eyes, limbs, head, paid is severe, or bruising is frequent.

📄 Stop Use and Ask a Doctor If 34 words ▾

Stop use and ask a doctor if symptoms persist for more than 3 days or get worse, new symptoms occur, or redness or swelling is present. These could be signs of a serious condition.

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant or breast-feeding, ask a health professional before use.

📄 Keep Out of Reach of Children 22 words ▾

Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 14 words ▾

Questions, Comments? BoironUSA.com [email protected] 1-800-BOIRON-1 (1-800-264-7661) Distributed by Boiron, Inc. Newtown Square, PA 19073-3267

📄 Package Label / Principal Display Panel 9 words ▾

LABEL LABEL LABEL LABEL LABEL LABEL LABEL LABEL LABEL

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Arnicare Procedure Recovery (this brand).

Top reported reactions

Fatigue10
Arthralgia9
Drug Hypersensitivity9
Headache9
Back Pain7
Pruritus7
Cardiac Disorder6

Age at onset

Adult6
Elderly9

Reporter sex

79 reports
Male · 20%
Female · 78%
Unknown · 1%

Serious outcomes

Hospitalization24
Life-threatening4
Death4
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 7 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing Kit / multi-component package

About homeopathic listings

Arnicare Procedure Recovery ARNICA MONTANA KIT 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.

Kit / multi-component package

This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.

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 Laboratoires Boiron. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Laboratoires Boiron 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.
← 00220-9049-42 · Laboratoires 00220-9053-43 · Boiron →
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.