Vicks Nyquil Severe Honey Liquid
FDA Label NDC 69423-968

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Procter & Gamble Manufacturing Company for the product Vicks Nyquil Severe Honey (NDC 69423-968). 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 ingredients (in each 15 ml), purpose, uses, liver warning, allergy alert:, sore throat warning, do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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