Onessip Adult Daytime Severe Cold And Flu Solution
FDA Label NDC 87078-972

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Medwise Lifesciences Inc. for the product Onessip Adult Daytime Severe Cold And Flu (NDC 87078-972). 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 onessip day time adult severe cold & flu 15 ml sachet drug facts, otc - purpose, indications & usage, warnings, otc - do not use, otc - ask doctor, otc - ask doctor/pharmacist, otc - when using, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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