All of the following statements are true regarding nonprescription drugs EXCEPT:

A. The FDA requires a Drug Facts label on packaging to standardize content and formatting for nonprescription labels: The FDA mandates a standardized Drug Facts label to ensure consumers can easily understand active ingredients, uses, warnings, and directions. This promotes safe self-medication and consistency across all OTC products. B. Packaging must be tamper-resistant: Nonprescription drugs are required to have tamper-evident packaging to protect consumers from contamination or product alteration. This regulation was strengthened to improve safety and ensure product integrity before use. C. Health care providers are needed to counsel patients on the safe and effective use of the products: OTC medications are specifically designed for self-care without the need for direct supervision by a healthcare provider. While counseling can improve safe use, it is not a requirement for consumers to access or use these medications. D. Consumers can use them for self-diagnosed conditions: A key feature of OTC medications is that they are intended for conditions that individuals can recognize and manage on their own. This allows timely treatment of minor illnesses without requiring a prescription.