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Minovia Mini Package Insert

Status:
Prescription (Rx) Facts
Strength:
1000 IU, 100 mg, 1000 IU, 20 mg, 1.67 mg, 100 mcg, 27 mg
Drug class:
Active ingredients:
Similar drugs:

Source: FDA drug labeling via NLM DailyMed · About this document

Prescribing information (package insert) - Minovia Mini

DESCRIPTION

Minovia Mini is a prescription multivitamin/multimineral dietary supplement.

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.

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

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.

DOSAGE AND ADMINISTRATION

Usual adult dose is 2 tablets by mouth once or twice daily as prescribed by a licensed medical practitioner.

HOW SUPPLIED

Bottles of 30 Tablets (85477-924-30). Tablet is tan, oval.

About this document

Source: FDA drug labeling via NLM DailyMed · View the label on DailyMed

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The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Minovia Mini

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Drug class Vitamin A, Vitamin B12, Vitamin C, Vitamin D
Active ingredients Vitamin A 1000 IU, Ascorbic acid 100 mg, Cholecalciferol 1000 IU, Thiamine 20 mg, Folic acid 1.67 mg, Cyanocobalamin 100 mcg, Ferrous fumarate 27 mg
Dosage form Tablet
Route Oral
Marketing status listed in the FDA NDC Directory
Company (applicant) Oncora Pharma, LLC
FDA approval UNAPPROVED DRUG OTHERUnapproved drug
Manufacturers 1 labelers list this drug on DailyMed
Packages (NDC)
Package
1000 IU, 100 mg, 1000 IU, 20 mg, 1.67 mg, 100 mcg, 27 mg – 30 in 1 bottle NDC 85477-924-30

Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.