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Signs of spoilage include color changes, separation, or a bad smell

The FDA will review the full meeting record After the meeting, the FDA can consider: The committees recommendations Written comments submitted to the public docket Public testimony presented during the meeting FDA staff evaluations Substance characterization and sourcing concerns Available human, animal, and laboratory research Additional regulatory or safety information The FDAs July 2026 briefing document states that the final determination may also be affected by issues that were not discussed during the public meeting

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Each batch is manufactured to meet or exceed 99% purity and verified by HPLC and LC-MS testing