Under what condition do labeling provisions not apply to dangerous drugs for food production animals?

Labeling provisions for dangerous drugs used in food production animals are primarily guided by regulatory standards to ensure consumer safety and proper drug usage. When federal requirements are met, it indicates that the drugs have been evaluated and approved by federal authorities, ensuring they meet safety and efficacy guidelines. In such cases, the stringent labeling provisions that typically apply may not be necessary, as compliance with federal standards provides a level of assurance that the drug will be used appropriately.

Other scenarios that may influence labeling requirements, such as the existence of a written directive, the origin of the drug, or the classification of the animals, do not necessarily negate the need for careful labeling. The focus here is on federal standards, which aim to unify regulations and provide a consistent basis for ensuring that drugs are safe for use in food production, thereby safeguarding public health.