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Code of Federal Regulations (Last Updated: July 5, 2024)

Title 21 - Food and Drugs

Chapter I - Food and Drug Administration, Department of Health and Human Services

SubChapter B - Food for Human Consumption

Part 111 - Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements

Subpart K - Production and Process Control System: Requirements for Manufacturing Operations

§ 111.370 - What requirements apply to rejected dietary supplements?

Latest version.

§ 111.370 What requirements apply to rejected dietary supplements?

You must clearly identify, hold, and control under a quarantine system for appropriate disposition any dietary supplement that is rejected and unsuitable for use in manufacturing, packaging, or labeling operations.

                    
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