BMNP AMBRA GRISEA
BMNP AMBRA GRISEA is an FDA drug label for the active ingredient AMBRA GRISEA 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
- AMBRA GRISEA
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 82969-5226
- Application
- N/A
- Label effective
- 20260901
About this product
BMNP AMBRA GRISEA is an FDA-registered drug product whose active ingredient is AMBRA GRISEA. 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 82969-5226, label effective 20260901. 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 AMBRA GRISEA are most often described in connection with: helps temporarily, relieve restlessness, muscle twitching, sensitivity cold, irritated sensitive. 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: restlessness, muscle twitching, sensitivity to cold, irritated or sensitive nerves
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.
Frequently asked questions
What is BMNP AMBRA GRISEA used for?
Helps temporarily relieve: restlessness, muscle twitching, sensitivity to cold, irritated or sensitive nerves
Who makes BMNP AMBRA GRISEA?
Total Operations Management LLC DBA:Bestmade Natural Products Micro is the labeler of record for BMNP AMBRA GRISEA.
What form does BMNP AMBRA GRISEA 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 AMBRA GRISEA 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.
Has BMNP AMBRA GRISEA 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.