What is a required component of a compounding record for non-sterile products?

In the context of compounding non-sterile products, a compounding record must include various essential components to ensure proper documentation and compliance with regulations. One key required component is quality control procedures. This aspect is crucial because it helps ensure the compounded product's consistency, purity, and overall quality. Including quality control procedures in the compounding record allows pharmacists to demonstrate adherence to established standards and provides a way to verify the process used during compounding.

Having these procedures documented supports the safety and effectiveness of the final product, which is paramount in pharmacy practice. It offers guidance on how to handle the ingredients and the process used, serving as a checklist for the pharmacists to confirm that all steps have been correctly followed.

While patient name, active ingredient cost, and insurance information might be relevant in different contexts, they do not fulfill the specific requirements set for the compounding record aimed at ensuring the quality of non-sterile products. The emphasis on quality control relates directly to preventing errors and ensuring that compounded medications are safe for patient use.