What are the restrictions regarding the labeling of drugs?

In Washington, there are specific restrictions surrounding the labeling of drugs. The Washington Administrative Code (WAC) requires prescription drugs to be labeled with information that includes the generic name of the drug, items such as directions on how to take the drug, a description of possible side effects, a warning of any potential hazards that might occur from taking the drug, and the name of the manufacturer. All of this information must be given in understandable language. In addition, the WAC requires all drugs to be properly labeled in a way that will not result in confusion for the consumer. This means that drug packages must be labeled with the name of the drug, the strength, the amount, a statement about the expiration date, the name of the manufacturer, and the name and address of the distributor. Manufacturers and distributors are also required to ensure that the labels have been approved by the Washington State Department of Health. Finally, all drug labels must include appropriate warnings and precautionary statements. These warnings are meant to alert consumers of the possible dangers associated with taking a drug. The warnings will vary depending on the type of drug and its effect on the consumer. These warnings might include statements such as informing consumers of potential drug interactions or possible side effects of taking a drug and cautions to not take a drug while pregnant or breastfeeding.

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