Minovia Mini
Minovia Mini is an FDA drug label for the active ingredient MINOVIA MINI manufactured by Oncora Pharma, LLC 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 20260624.
- Generic name
- MINOVIA MINI
- Manufacturer
- Oncora Pharma, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 85477-924
- Application
- N/A
- Label effective
- 20260624
About this product
Minovia Mini is an FDA-registered drug product whose active ingredient is MINOVIA MINI. It is labelled by Oncora Pharma, LLC taken by oral and marketed as a human prescription drug product. Identifiers on file: NDC 85477-924, label effective 20260624. 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 MINOVIA MINI are most often described in connection with: usage minovia, mini prescription, multivitamin multi-mineral, dietary supplement, management suboptimal, nutritional status, advanced folate, vitamin supplementation. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Indications & Usage
INDICATIONS AND USAGE Minovia Mini is a prescription multivitamin/multi-mineral dietary supplement formulated for the clinical dietary management of a suboptimal nutritional status in patients where advanced folate, vitamin B supplementation, and maintenance of good health is needed.
Dosage & Administration
DOSAGE AND ADMINISTRATION Usual adult dose is 2 tablets by mouth once or twice daily as prescribed by a licensed medical practitioner.
Warnings
WARNINGS Accidental overdose of iron-containing products is a leading cause of fatal poising in children under 6. KEEP THIS PRODUCT OUT OF REACH OF CHILDREN. In the case of accidental overdose, call a doctor or poison control center immediately.
Adverse Reactions
ADVERSE REACTIONS Allergic sensitization has been reported following both oral and parenteral administration of folic acid. You should call your doctor for medical advice about serious adverse events. To reports adverse side effects or to obtain product information, contact Oncora Pharma at 888-321-2821.
Frequently asked questions
What is Minovia Mini used for?
INDICATIONS AND USAGE Minovia Mini is a prescription multivitamin/multi-mineral dietary supplement formulated for the clinical dietary management of a suboptimal nutritional status in patients where advanced folate, vitamin B supplementation, and maintenance of good health is needed.
Who makes Minovia Mini?
Oncora Pharma, LLC is the labeler of record for Minovia Mini.
What form does Minovia Mini 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 Minovia Mini prescription or over-the-counter?
The FDA label for this product is recorded as human prescription drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has Minovia Mini 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.