Daytime Nighttime Cold Flu Relief Kit
FDA Label NDC 68016-799

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Chain Drug Consortium, Llc for the product Daytime Nighttime Cold Flu Relief (NDC 68016-799). 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 active ingredients for daytime (in each softgel), active ingredients for nighttime (in each softgel), purpose for daytime, purpose for nighttime, uses, warnings, 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.

* Please review the disclaimer below.