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Bionara ULTRA

Generic: Probiotic Dietary Supplement Capsules

Verified·Apr 23, 2026
NDC
85477-710
Route
ORAL
ICD-10 indication
K59.9

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About Bionara ULTRA

What is this medication? Bionara ULTRA is not currently listed as a standard or FDA-approved prescription medication in major medical and pharmaceutical databases. Because this name does not match any recognized clinical drug, it is possible the product is a dietary supplement, a cosmetic formulation, or a brand-specific wellness product that is not regulated as a prescription medicine. As there is no official clinical record for a medication under this name, its specific therapeutic uses and benefits are not documented in professional medical literature.

If you have been advised to take this product, it is essential to review the label for its active ingredients and consult with a healthcare professional before use. Relying on substances that are not verified by medical authorities can be hazardous to your health and may lead to complications or adverse drug interactions. Always ensure that any treatment you use is prescribed by a licensed provider and sourced from a reputable pharmacy to guarantee its safety and efficacy.

Copay & patient assistance

Detailed copay and financial assistance information is not publicly available for this medication at this time. Please consult your pharmacist or the manufacturer's official patient support program for more details.

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Prescribing information

From the FDA-approved label for Bionara ULTRA. Official source: DailyMed (NLM) · Label effective Feb 25, 2026

Indications and usage
INDICATIONS AND USAGE Bionara Ultra™ is a prescription probiotic supplement intended to support gastrointestinal health and maintain normal intestinal flora balance. Dispensed by prescription under medical supervision.
Dosage and administration
DOSAGE AND ADMINISTRATION Usual adult dose is 2 capsules once or twice daily or as prescribed by a licensed medical practitioner.
Contraindications
CONTRAINDICATIONS None known.
Warnings
WARNINGS Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6. In case of accidental overdose, call a doctor or poison control center immediately. If pregnant, lactating, or trying to conceive, consult with a licensed healthcare professional prior to use.

Label text is reproduced as-is from the FDA-approved label. We do not paraphrase, summarize, or omit. Content above is for informational purposes only and is not medical advice. Always consult your prescribing clinician or pharmacist before making decisions about your medication.

Conditions we've indexed resources for

Click a condition to see copay cards, grants, and PA rules specific to it. For the full list of FDA-approved indications, see Prescribing information above.

Prior authorization & coverage

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Medicare Part D

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How this page is sourced

  • Drug identity verified against openFDA NDC Directory.
  • Label text (when shown) originates from NLM DailyMed.
  • Copay and assistance URLs verified periodically; if you hit a broken link, tell us.