The U.S. Department of Agriculture (USDA) defines honey as “a sweet, syrupy substance produced by honey bees from the nectar of plants or from secretions of living parts of plants or excretions of plant-sucking insects on the living part of plants, which the bees collect, transform by combining with specified substances of their own, deposit, dehydrate, store, and leave in the honeycombs to ripen and mature.” Honey has specific regulations based on where it is produced, but in the United States it is one of the foodstuffs governed both by the Food and Drug Administration (FDA) and the USDA. The FDA restricts products marketing themselves as honey of any kind of floral origin to only those without additives. If a product has added sugar, flavor or chemical substitute, it cannot be called honey exclusively. It must identify the other substances both in the product name and in the ingredient list. The USDA has more stringent requirements, mandating that honey products identify the “type(s), source(s), floral source(s), preparation(s), color(s), grade(s), and agricultural practice(s) of the honey desired,” along with the results of a variety of authenticity tests in the commercial description of the product. If the product does not have a USDA classification as listed (based on a list of twenty-six different possible features that combine to make up the three-hundred-and-twenty recognized varieties of honey) or does not pass the required analysis, it cannot be considered honey.