BMNP ARGENTUM NITRICUM
BMNP ARGENTUM NITRICUM is an FDA drug label for the active ingredient ARGENTUM NITRICUM manufactured by Total Operations Management LLC DBA:Bestmade Natural Products Micro 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 20260901.
- Generic name
- ARGENTUM NITRICUM
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 82969-5233
- Application
- N/A
- Label effective
- 20260901
About this product
BMNP ARGENTUM NITRICUM is an FDA-registered drug product whose active ingredient is ARGENTUM NITRICUM. It is labelled by Total Operations Management LLC DBA:Bestmade Natural Products Micro taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 82969-5233, label effective 20260901. It is one of 5 FDA drug label records sharing the active ingredient ARGENTUM NITRICUM. 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 ARGENTUM NITRICUM are most often described in connection with: helps temporarily, relieve digestive, anxiousness trembling, nervous tension, weakness nervousness. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Helps temporarily relieve: digestive upset from anxiousness, trembling from nervous tension, weakness, nervousness
Dosage & Administration
Use as directed. Take with water, 3-4 times daily. Ages 12 and older: 2 pellets. Ages 3 to 11: 1 pellet. Ages below 3: consult your doctor.
Warnings
Keep out of reach of children. If pregnant or breastfeeding, ask a health professional before use. Stop use and ask a doctor if symptoms persist or worsen. If you have severe symptoms, consult a doctor before use.
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View labelHow products containing ARGENTUM NITRICUM compare
FDA lists 5 drug label records with ARGENTUM NITRICUM 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 |
|---|---|---|---|
| — | — | Hahnemann Laboratories, Inc. | 1 |
| — | — | Natural Immunogenics Corp.dba SOVEREIGN NATURALS | 1 |
| — | — | Rxhomeo Private Limited d.b.a. Rxhomeo, Inc | 1 |
| — | — | Total Operations Management LLC DBA:Bestmade Natural Products Micro | 1 |
| — | — | True Botanica, LLC | 1 |
Frequently asked questions
What is BMNP ARGENTUM NITRICUM used for?
Helps temporarily relieve: digestive upset from anxiousness, trembling from nervous tension, weakness, nervousness
Who makes BMNP ARGENTUM NITRICUM?
Total Operations Management LLC DBA:Bestmade Natural Products Micro is the labeler of record for BMNP ARGENTUM NITRICUM. 5 FDA label records share the active ingredient ARGENTUM NITRICUM, 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 BMNP ARGENTUM NITRICUM 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 BMNP ARGENTUM NITRICUM 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 ARGENTUM NITRICUM?
Yes. 5 FDA drug label records list ARGENTUM NITRICUM 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 BMNP ARGENTUM NITRICUM 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.