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Virexa Package Insert

Status:
Prescription (Rx) Facts
Strength:
125 mg, 12.5 mcg, 25 mg, 125 mg, 1.667 mg, 1 mg, 5 mg, 50 mg
Drug class:

Prescribing information (package insert) - Virexa

Usual Adult dose is 1 tablet once or twice daily or as prescribed by a licensed medical practitioner.

Accidental overdose of iron-containing products is a leading cause of fatal poisoninng in children under 6.

Keep out of reach of children.

In case of accidental overdose, call a doctor or poison control immediately.

Virexa is a multivitamin with folic acid dispensed by prescription only.

Store at 20°-25° C (68°-77°F) exursions permitted to 15°-30°C (59°F-86°F). Keep in cool dry place. [See USP Controlled Room Temperature] Avoid excessive heat, light, moisture and exceeding 85% humidity.

Active Ingredients: VItamin C, Vitamin D3, Vitamin B1, Vitamin B6, Vitamin B12, Folic Acid, NADH, Ubiquinone.

Inactive Ingredients: Microcrystalline Cellulose, Pregeleatinized Starch, Coating (Beta-Carotene, Titanium Dioxide, Hypromellose, Polyvinyl Alcohol, Polyethylene Glycol, Talc), Croscarmellose Sodium, Silica, Silicon Dioxide, Hydroxypropyl Cellulose, Magnesium Stearate.

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 Virexa

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Drug class Vitamin C, Vitamin D
Active ingredients Ascorbic acid 125 mg, Cholecalciferol 12.5 mcg, Thiamine hcl 25 mg, Pyridoxal phosphate anhydrous 125 mg, Folic acid 1.667 mg, Methylcobalamin 1 mg, Nicotinamide adenine dinucleotide 5 mg, Ubiquinone 50 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
125 mg, 12.5 mcg, 25 mg, 125 mg, 1.667 mg, 1 mg, 5 mg, 50 mg – 30 in 1 bottle NDC 85477-606-30

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.