Arnica Recovery

Arnica Recovery is an FDA-registered drug product whose active ingredient is ARNICA MONTANA. It is labelled by NARTEX LABORATORIOS HOMEOPATICOS SA DE CV taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 34666-010, label effective 20180227. 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.

Across FDA labelling, products containing ARNICA MONTANA are most often described in connection with: homeopathic materia, temporary relief, sore muscles, bruises sprains, medica product, evaluated teh, drug administration, clinically tested. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

For the temporary relief of sore muscles bruises sprains as per homeopathic materia medica Product uses are based on Homeopathic Materia Medica. These "Uses" have not been evaluated by teh Food and Drug Administration. This product has not been clinically tested by Nartex Labs USA, Inc.

Directions: adults and children 4 years of age and older: take 2 tablets every 6 hours, slowly dissolving in mouth children under 4 years of age: consult a physician

Do not use if you have an allergy or hypersensitivity to the components of the formula.

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.

What is Arnica Recovery used for?
For the temporary relief of sore muscles bruises sprains as per homeopathic materia medica Product uses are based on Homeopathic Materia Medica. These "Uses" have not been evaluated by teh Food and Drug Administration. This product has not been clinically tested by Nartex Labs USA, Inc.

Who makes Arnica Recovery?
NARTEX LABORATORIOS HOMEOPATICOS SA DE CV is the labeler of record for Arnica Recovery. 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 Recovery 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 Recovery 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 Recovery 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.