Biofreeze Overnight Gel
FDA Label NDC 59316-121

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Reckitt Benckiser Llc for the product Biofreeze Overnight Gel (NDC 59316-121). 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 warnings, directions, other info, inactive ingredients, otc - questions, drug facts, uses, active, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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