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And http://www.fda.gov/AboutFDA/AboutThisWebsite/WebsitePolicies/default.htm. FORM FDA 3852 (6/16). Page 1 of 3. PSC Publishing Services (301) .

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How to fill out the FDA 3852 online

The FDA 3852 form is essential for reporting tobacco product removals subject to tax and is required for user fee assessments. This guide will provide clear, step-by-step instructions on how to complete the form accurately and efficiently in an online format.

Follow the steps to fill out the FDA 3852 form online.

  1. Press the ‘Get Form’ button to access the FDA 3852 form and open it in the designated editor.
  2. Enter your company name and address, including the zip code, in the first section. If there is an alternate address for FDA notifications, provide that information as well.
  3. Provide the name of the contact person responsible for this submission.
  4. Fill in the TTB permit number associated with your company.
  5. Include the telephone number, ensuring you include the appropriate area code.
  6. Enter your Employer Identification Number (EIN) clearly to ensure proper identification.
  7. Fill in the email address for correspondence regarding this form.
  8. Specify the period of activity by selecting the appropriate month and year from the provided options.
  9. In the 'Domestic taxable removals' section, input the volume and taxes for each tobacco product category, including cigarettes, cigars, snuff, chewing tobacco, pipe tobacco, and roll-your-own tobacco, as per the instruction given in the boxes and lines.
  10. Complete the certification section by printing and signing your name, stating your title, and entering the date this form was prepared.
  11. Once the form is completely filled out, save your changes, and then you can download, print, or share the completed form as required.

Start completing your FDA 3852 form online today to ensure compliance with user fee regulations.

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The term “tobacco product” means any product made or derived from tobacco that is intended for human consumption, including any component, part, or accessory of a tobacco product (except for raw materials other than tobacco used in manufacturing a component, part, or accessory of a tobacco product).

FDA's Center for Tobacco Products regulates the following tobacco products: Cigarettes. Cigars. Dissolvables. Hookah Tobacco. Nicotine Gels. Non-Tobacco Nicotine. Pipe Tobacco. Roll-Your-Own Tobacco.

In April 2022, FDA announced proposed product standards to prohibit menthol as a characterizing flavor in cigarettes and to prohibit characterizing flavors (other than tobacco flavor) in cigars. When finalized, these product standards are expected to significantly reduce initiation and increase cessation.

The Deeming Rule extends the FDA's authority to regulate tobacco products to include electronic nicotine delivery systems (such as e-cigarettes and vape pens), all cigars, hookah (waterpipe) tobacco, pipe tobacco, and nicotine gels.

To protect Americans from tobacco-related disease and death, FDA provides information about tobacco products, including cigarettes, and the dangers they pose to the public. The harmful chemicals in cigarette smoke can damage nearly every organ in the body.

Yes, FDA regulates NTN products. Since passage of the Family Smoking Prevention and Tobacco Control Act (commonly called the Tobacco Control Act) in 2009, FDA has regulated the manufacturing, distribution, and marketing of tobacco products.

Tobacco products encompass varieties of products including cigarettes, cigarette tobacco, roll-your-own tobacco, smokeless tobacco, electronic cigarettes, cigars, hookahs, pipe tobacco, nicotine gels, and dissolvables.

The term “tobacco product” means any product made or derived from tobacco that is intended for human consumption, including any component, part, or accessory of a tobacco product (except for raw materials other than tobacco used in manufacturing a component, part, or accessory of a tobacco product).

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