Dosage & Administration
Usual Adult dose is 1 tablet once or twice daily or as prescribed by a licensed medical practitioner.
Virexa Tablet
FDA Label NDC 85477-606
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Oncora Pharma, Llc for the product Virexa (NDC 85477-606). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding dosage & administration, warnings, indications & usage, how supplied, description, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
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.
Indications & Usage
Virexa is a multivitamin with folic acid dispensed by prescription only.
How Supplied
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.
Description
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.
Package Label.Principal Display Panel
Label (Virexa Oncora)
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