Uqora Maximum Uti Pain Relief And Flush Convenience Bundle Kit
FDA Label NDC 73712-600

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bonafide Health, Llc Dba Uqora for the product Uqora Maximum Uti Pain Relief And Flush Convenience Bundle (NDC 73712-600). 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 uqora maximum uti pain relief, active ingredient (in each tablet), purpose, use, warnings, do not use, ask a doctor before use, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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