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Regulation 1151/2012 on quality schemes for agricultural products and foodstuffs: defines "labelling" as "any words, particulars, trade marks, brand name, pictorial matter or symbol relating to a foodstuff and placed on any packaging, document, notice, label, ring or collar accompanying or referring to such foodstuff".
The Fair Packaging and Labeling Act required all "consumer commodities" to have a label. Under the act, consumer commodities were defined as any food, drug, device, or cosmetic, that is produced or distributed for sale through retails sales/agencies for consumption by individuals or used by individuals for the purpose of personal care.
Warning label on a cigarette pack: "Smoking kills". Warning label for a personal watercraft. Warning label for toxic chemicals. A warning label is a label attached to a product, or contained in a product's instruction manual, warning the user about risks associated with its use, and may include restrictions by the manufacturer or seller on certain uses.
The US Food and Drug Administration has finalized new standards that foods must meet before they can be labeled as “healthy.” ...
New York City residents may soon see warning labels next to sugary foods and drinks in chain restaurants and coffee shops, under a law set to go into effect later this year. The rule requires food ...
Mandatory labelling is mandated in most developed nations and increasingly also in developing nations, especially for food products, e.g. "Grade A" meats. With regard to food and drugs, mandatory labelling has been a major battleground between consumer advocates and corporations since the late 19th century.
In Israel, there’s a red warning label on such food and drinks. ... The statistics don’t mean that the nutrition facts box that became required on the backs or sides of food packaging three ...
"Nutrition Facts Label Programs & Materials". Ingredients, Packaging & Labeling. Labeling & Nutrition. U.S. Food and Drug Administration. Nutritional Health Alliance v. Shalala, 953 F.Supp. 526 (S.D.N.Y., 1997) Challenge, on First Amendment grounds, the NLEA framework requiring advanced FDA authorization for health claims made on vitamin labels.