Alka-seltzer Plus Severe Cold Powerfast Fizz Kit
FDA Label NDC 0280-0025

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bayer Healthcare Llc. for the product Alka-seltzer Plus Severe Cold Powerfast Fizz (NDC 0280-0025). 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 product, drug facts, active ingredients, uses, warnings, do not use, ask a doctor, ask a doctor or pharmacist, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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