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Headlines Tagged with Federal/National 16,332 headlines found

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WARNING LETTER: Swisher International, Inc.

FDA has determined that your Swisher Sweets Grape products labeled as “little cigars” meet the FD&C Act’s definition of “cigarettes.”...also determined that your Swisher Sweets Grape cigarette products are adulterated under section 902(5) of the FD&C Act
Food and Drug Administration (FDA)
added Dec 10, 2016 00:50
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Registration and Listing Guidance Revised with New Compliance Period

companies which begin manufacturing newly regulated tobacco products in a domestic establishment on or after the August 8 effective date of the deeming rule must register and list immediately with the FDA. The FDA is currently accepting submissions and e
Food and Drug Administration (FDA)
added Dec 10, 2016 00:47
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Warning Letters Sent to Four Tobacco Product Manufacturers

FDA determined that the products are adulterated because they contain a natural or artificial characterizing flavor, or misbranded if they only purport to do so. Read the Warning Letters
Food and Drug Administration (FDA)
added Dec 10, 2016 00:46
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Health Document Submission Requirements for Tobacco Products (PDF)

(a) Requirement—Each tobacco product manufacturer or importer, or agents thereof, shall submit to the Secretary the following information: . . . . (4) Beginning 6 months after the date of enactment of the Family Smoking Prevention and Tobacco Cont
Food and Drug Administration (FDA)
added Dec 9, 2016 23:33
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Tobacco Health Document Submission

Who should submit health documents FDA’s compliance policies What information to include in health document submissions How to make health document submissions When to make health document submissions
Food and Drug Administration (FDA)
added Dec 9, 2016 23:30
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Registration and Product Listing for Owners and Operators of Domestic Tobacco Product Establishments (Revised*) Guidance for Industry (PDF)

Every person who owns or operates any domestic establishment engaged in manufacturing regulated tobacco products must register under section 905(b) of the FD&C Act, and every registrant must file a list of its regulated tobacco products in accordance wit
Food and Drug Administration (FDA)
added Dec 9, 2016 23:28
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Registration and Product Listing for Owners and Operators of Domestic Tobacco Product Establishments

This guidance document is intended to assist owners and operators of domestic tobacco product establishments with the registration and product listing submissions required by section 905 of the Food, Drug, and Cosmetic Act (FD&C Act). The guidance docume
Food and Drug Administration (FDA)
added Dec 9, 2016 23:27
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FDA takes action against four tobacco manufacturers for illegal sales of flavored cigarettes labeled as little cigars or cigars

The companies received warning letters for products under the “Swisher Sweets,” Cheyenne,” “Prime Time” and “Criss-Cross” brands in a variety of youth-appealing flavors, including grape, cherry, wild cherry and strawberry.
Food and Drug Administration (FDA)
added Dec 9, 2016 22:07
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Tobacco Marketing Presents Persistent Challenges for Health Experts

"The images that the FDA proposed were very similar to other graphic images that we have seen being used in warning labels in other countries around the world." However, the tobacco industry challenged those images and won the lawsuit. So now the FDA i
Time Warner Cable News
added Dec 9, 2016 22:01
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[Pennsylvania] EDITORIAL: Our view: Smoking ban clears air, saves money

Numbers provided by the government make a sound, convincing case for the ban, especially when the interests of taxpayers are factored in.
Erie (PA) Times-News
added Dec 9, 2016 21:38
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