Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride Syrup
FDA Label NDC 0031-8729

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Haleon Us Holdings Llc for the product Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride (NDC 0031-8729). 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 principal display panel - shipping label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.