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Federal Register / Vol. 68, No. 77 / Tuesday, April 22, 2003 / Notices
Because of the limited timeframes
established by section 510(m) of the act,
FDA has determined, under
10.115(g)(2) (21 CFR 10.115(g)(2)),
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How to fill out deeming tobacco products to
01
Identify the type of tobacco product being deemed.
02
Complete all required fields on the deeming tobacco products form.
03
Provide any supporting documentation that may be required.
04
Submit the completed form to the appropriate regulatory agency.
Who needs deeming tobacco products to?
01
Manufacturers and importers of tobacco products who are seeking to have their products deemed by regulatory agencies.
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What is deeming tobacco products to?
Deeming tobacco products refers to the action taken by regulatory authorities to classify certain products, such as e-cigarettes and vaping products, under the same regulations that apply to traditional tobacco products.
Who is required to file deeming tobacco products to?
Manufacturers, importers, and distributors of tobacco products that fall under the deeming rule are required to file the necessary documentation with the relevant regulatory body.
How to fill out deeming tobacco products to?
To fill out the deeming tobacco products documentation, submit required forms that include product details, compliance data, and any supporting documentation as specified by the regulatory authority.
What is the purpose of deeming tobacco products to?
The purpose of deeming tobacco products is to extend regulatory oversight to new products, ensuring safety, quality, and accurate information for consumers regarding tobacco and nicotine use.
What information must be reported on deeming tobacco products to?
Information required for deeming tobacco products includes product identification, manufacturing details, health information, ingredients, and marketing practices.
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