What must be recorded when compounding non-sterile products?

When compounding non-sterile products, it is essential to document the components used, the quantities of each ingredient, and the process steps involved in the compounding procedure. This thorough documentation ensures the reproducibility of the compounded preparation and validates that the product meets the required specifications for safety, efficacy, and quality.

Recording the components and their respective quantities helps in verifying the formulation and allows for accurate replication in future compounding. Additionally, detailing the process steps provides important information on the techniques applied during the compounding, which can affect the final product's integrity and effectiveness. Comprehensive records are not only crucial in complying with regulatory requirements but also play a vital role in maintaining a high standard of practice in pharmacy operations.