BMNP AMMONIUM CARBONICUM
BMNP AMMONIUM CARBONICUM is an FDA drug label for the active ingredient AMMONIUM CARBONICUM 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
- AMMONIUM CARBONICUM
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 82969-5227
- Application
- N/A
- Label effective
- 20260901
About this product
BMNP AMMONIUM CARBONICUM is an FDA-registered drug product whose active ingredient is AMMONIUM CARBONICUM. 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 82969-5227, label effective 20260901. It is one of 3 FDA drug label records sharing the active ingredient AMMONIUM CARBONICUM. 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 AMMONIUM CARBONICUM are most often described in connection with: helps temporarily, relieve fatigue, sensitivity cold, sluggish circulation, respiratory discomfort. 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: fatigue, sensitivity to cold, sluggish circulation, respiratory discomfort
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.
More products with the same ingredient
AMMONIUM CARBONICUMHow products containing AMMONIUM CARBONICUM compare
FDA lists 3 drug label records with AMMONIUM CARBONICUM 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 |
| — | — | Rxhomeo Private Limited d.b.a. Rxhomeo, Inc | 1 |
| — | — | Total Operations Management LLC DBA:Bestmade Natural Products Micro | 1 |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is BMNP AMMONIUM CARBONICUM used for?
Helps temporarily relieve: fatigue, sensitivity to cold, sluggish circulation, respiratory discomfort
Who makes BMNP AMMONIUM CARBONICUM?
Total Operations Management LLC DBA:Bestmade Natural Products Micro is the labeler of record for BMNP AMMONIUM CARBONICUM. 3 FDA label records share the active ingredient AMMONIUM CARBONICUM, 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 AMMONIUM CARBONICUM 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 AMMONIUM CARBONICUM 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 AMMONIUM CARBONICUM?
Yes. 3 FDA drug label records list AMMONIUM CARBONICUM 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 AMMONIUM CARBONICUM 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.