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A.h'lb DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration Docket Nos. 92P-0274 and 97P-0437 Determination That Benedictine Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness
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Ahlb - FDA stands for Animal and Human Food Biotechnology and Labeling Act - Food and Drug Administration. It is a regulation enforced by the FDA that requires certain food products to be labeled if they contain or are derived from genetically engineered ingredients.
Manufacturers, distributors, and importers of food products that contain or are derived from genetically engineered ingredients are required to file ahlb - fda.
To fill out ahlb - fda, the responsible party needs to provide information on the genetically engineered ingredients used in the food product, including their purpose and potential allergenicity. They also need to provide accurate labeling information to inform consumers about the presence of genetically engineered ingredients.
The purpose of ahlb - fda is to ensure transparency and consumer awareness regarding the use of genetically engineered ingredients in food products. It aims to provide consumers with information about the presence and nature of genetically engineered ingredients, allowing them to make informed choices when purchasing and consuming food.
On ahlb - fda, the responsible party must report details of genetically engineered ingredients used in the food product, including their purpose, potential allergenicity, and accurate labeling information.
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