What documentation must a compounding record contain?

The compounding record must contain the formula and preparation details of the compounded drug. This documentation is crucial for several reasons. First, it ensures that there is a clear and detailed account of how the compounded medication was created, including the specific ingredients used, their quantities, and the exact procedure followed. This allows for consistency in preparation and helps to maintain quality control in the compounding process.

Moreover, these records are vital for traceability and accountability. Should any issues arise with the compounded product, the compounding record provides the necessary information to investigate any potential problems or recalls. Furthermore, having thorough documentation aids in compliance with regulatory requirements set forth by state boards and the FDA, ensuring that pharmacies adhere to safe compounding practices.

In terms of the other options: they do not provide the essential and comprehensive information required for safety, quality assurance, and regulatory compliance in compounding.