Arnica Montana 30X HPUS
Arnica Montana 30X HPUS is an FDA drug label for the active ingredient ARNICA MONTANA manufactured by VITAMEDICA, INC. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260608.
- Generic name
- ARNICA MONTANA
- Manufacturer
- VITAMEDICA, INC.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 80004-005
- Application
- N/A
- Label effective
- 20260608
About this product
Arnica Montana 30X HPUS is an FDA-registered drug product whose active ingredient is ARNICA MONTANA. It is labelled by VITAMEDICA, INC. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 80004-005, label effective 20260608. It is one of 23 FDA drug label records sharing the active ingredient ARNICA MONTANA. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing ARNICA MONTANA are most often described in connection with: temporarily relieves, symptoms bruising, swelling pain, stiffness muscle, soreness claims, based traditional, homeopathic practice, accepted medical. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
USES: *Temporarily relieves these symptoms: • Bruising • Swelling • Pain • Stiffness • Muscle Soreness *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Dosage & Administration
DIRECTIONS: • Do not handle the tablets. Instead, drop tablets directly under the tongue and let dissolve naturally. Adults and children 12 years and over - Take 3 tablets, 3 times a day Children under 12 years - Not intended
Warnings
WARNINGS: Ask a doctor before use if pregnant or breastfeeding. Stop use or consult a physician if • Any adverse reactions occur • Symptoms persist for more than 14-days or worsen Keep this and all medications out of reach of children. In case of an emergency or accidental overdose, contact a medical professional or Poison Control immediately. CONTAINS: Lactose (milk) • Do not use if seal is broken or shows any signs of tampering. • Store at 68-77°F (20-25°C)
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View labelHow products containing ARNICA MONTANA compare
FDA lists 23 drug label records with ARNICA MONTANA as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Boiron | 3 |
| — | — | Laboratoires Boiron | 3 |
| — | — | Natural Creations, Inc. | 2 |
| — | — | VITAMEDICA, INC. | 2 |
| — | — | Beautivity LLC | 1 |
Frequently asked questions
What is Arnica Montana 30X HPUS used for?
USES: *Temporarily relieves these symptoms: • Bruising • Swelling • Pain • Stiffness • Muscle Soreness *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Who makes Arnica Montana 30X HPUS?
VITAMEDICA, INC. is the labeler of record for Arnica Montana 30X HPUS. 23 FDA label records share the active ingredient ARNICA MONTANA, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does Arnica Montana 30X HPUS come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Arnica Montana 30X HPUS prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Are there other products containing ARNICA MONTANA?
Yes. 23 FDA drug label records list ARNICA MONTANA as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has Arnica Montana 30X HPUS been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.