Guaifenesin Liquid
FDA Label NDC 72162-2278

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bryant Ranch Prepack for the product Guaifenesin (NDC 72162-2278). 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, active ingredient (in each 5 ml), purpose, uses, ask a doctor before use if you have, when using this product, stop use and ask a doctor if, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

How Supplied

Guaifenesin Liquid USP 100 mg/5 mL

  • NDC 72162-2278-2: Bottle of 16 fl. oz. (473 mL) 
  • Repackaged/Relabeled by:
    Bryant Ranch Prepack, Inc.
    Burbank, CA 91504

Package Label.Principal Display Panel

Guaifenesin Liquid 100 mg/5 mL

Label (Lbl721622278)

Label (Lbl721622278)

* Please review the disclaimer below.