Rhode Island Multistate Pharmacy Jurisprudence (MPJE) Practice Exam

Which two items must all compounded medications list on their labels?

1. Dosage and expiration date

2. Active ingredients and manufacturing date

3. Active ingredients and BUD

4. Ingredients and storage conditions

The correct answer is: Active ingredients and BUD

Compounded medications are subject to specific labeling requirements to ensure patient safety and accurate information regarding the product. The correct answer highlights the necessity of including both active ingredients and the beyond-use date (BUD) on labels. Active ingredients are essential to list because they inform the patient and healthcare providers about what therapeutic components are present in the compounded medication, which is crucial for understanding its effectiveness and ensuring patient safety, especially for those with allergies or sensitivities. The beyond-use date is critical as it indicates the time frame within which the compounded medication should be used to ensure its potency and safety. This is vital because compounded medications typically do not have the same stability as commercially manufactured products, meaning they can degrade or lose efficacy over time. Other choices may include important information but fail to encapsulate both the key active components and the safety timeframe in terms of usability. For instance, while dosage and expiration dates are relevant for many medications, they do not specifically cover compounded products' needs. Similarly, listing manufacturing dates or storage conditions, while important in their contexts, do not fulfill the requirement to specify active ingredients and their use timeframe comprehensively.