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  2. Fair Packaging and Labeling Act - Wikipedia

    en.wikipedia.org/wiki/Fair_Packaging_and...

    The Fair Packaging and Labeling Act is a U.S. law that applies to labels on many consumer products. It requires the label to state: The identity of the product; The name and place of business of the manufacturer, packer, or distributor; and; The net quantity of contents. The contents statement must include both metric and U.S. customary units.

  3. FDA wants food companies to put nutrition labels on the front ...

    www.aol.com/news/fda-wants-food-companies-put...

    Nancy Brown, CEO of the American Heart Association, said the FDA’s proposal for a front-facing nutrition label is “an important step to make nutrition information clearer and more accessible.”

  4. The Fascinating Backstory Behind Red Dye No. 3 - AOL

    www.aol.com/fascinating-backstory-behind-red-dye...

    Back then, the FDA reportedly considered banning the dye in foods too, but chose not to (more on why soon). The basis of both bans is the Delaney Clause , a federal law that was enacted in 1958.

  5. Red Dye 3 Just Got Banned. These Are the Foods to Avoid If ...

    www.aol.com/red-dye-3-just-got-134800003.html

    The Food and Drug Administration (FDA) has revoked the use of Red Dye No. 3 (also known as erythrosine, Red Dye 3, FD&C Red No. 3 and Red No. 3) in food and ingested drugs as of January 15 ...

  6. Nutrition labels may come to the front of food packages under ...

    www.aol.com/nutrition-labels-may-come-front...

    The US Food and Drug Administration is proposing nutrition information be placed on the front of packaged foods to provide at-a-glance information about saturated fat, sodium and added sugar.

  7. Drug expiration - Wikipedia

    en.wikipedia.org/wiki/Drug_expiration

    Manufacturers print expiration dates on drug bottle labels. [4] The labeled expiration date is a manufacturer's promise for a time until which the drug will have full efficacy and be safe as manufactured. [4] The labeled expiration date is not an indication of when a drug has become ineffective or unsafe to use. [4]

  8. America’s Most Admired Lawbreaker - The Huffington Post

    highline.huffingtonpost.com/miracleindustry/...

    The FDA orders a label change for Risperdal, specifying that it be used only for schizophrenia rather than the broader category of “psychotic disorders.” Meanwhile, the company accelerates its promotional efforts to children and the elderly, including giving pediatricians Legos that say “Risperdal” on them.

  9. Boxed warning - Wikipedia

    en.wikipedia.org/wiki/Boxed_warning

    In the United States, a boxed warning (sometimes "black box warning", colloquially) is a type of warning that appears near the beginning of the package insert for certain prescription drugs, so called because the U.S. Food and Drug Administration specifies that it is formatted with a 'box' or border around the text [1] to emphasize it is of ...