What essential information must labels for single compounded preparations include?

The essential information that labels for single compounded preparations must include is the name and amount of ingredients, beyond use date (BUD), and storage requirements. This information is crucial for ensuring the safe and effective use of the compounded medication.

Including the name and amount of ingredients allows healthcare providers to verify the formulation and ensure that it was prepared correctly. The BUD is critical as it indicates the period within which the compounded preparation should be used to maintain its efficacy and safety, which protects patient health. Moreover, storage requirements indicate the appropriate conditions for maintaining the stability and integrity of the preparation, ensuring that it remains effective when administered to the patient.

While information about the prescribing physician, patient information, the compounding technician's name, and pharmacy registration number are important in various contexts, they are not universally required on every compounded preparation label. The focus of a compounded preparation label is primarily on the preparation itself to ensure its correct handling and use. Therefore, the details concerning the ingredients, BUD, and storage are fundamental in the labeling process for safety and compliance with regulations.