Axiv Daytime Capsule, Liquid Filled
FDA Label NDC 82706-015

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Vivunt Pharma Llc for the product Axiv Daytime (NDC 82706-015). 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 other, otc - purpose, uses, liver warning, allergy alert, sore throat warning, do not use, ask a doctor before use if you have, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Overdose Warning

In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately.

* Please review the disclaimer below.