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Web Content Syndication – Web Pages

Exchange Lab offers free, high-quality tobacco prevention content for your website. This page contains content from FDA's web pages that you can place on your website using our syndication tool. Once you place the code on your site, syndicated content is automatically updated whenever the content is changed on the FDA site. To get started, see Exchange Lab Digital Content: Publishing Instructions. If you have questions, please contact us for help.

52 results

How Do I Report a Vape Battery Explosion to FDA?

FDA is aware of explosion events and is collecting data to help address this problem.
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Pregnancy and Smoking

There is no safe level of exposure to secondhand smoke.
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Secondhand Smoke

Most tobacco use begins during adolescence.
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Youth and Tobacco

Tobacco has serious effects on the health of users.
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Health Effects of Tobacco Use

Tobacco has serious effects on the health of users.
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Q&A with CTP’s Director of Communications

Kathy Crosby is the Director of the Center for Tobacco Products (CTP) Office of Health Communication and Education. This multidisciplinary office contains several specialized divisions and teams, including regulatory communications, public...
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The Freedom of Information Act

In conducting its work as an agency of the federal government, FDA creates and generates documents, and the public may request these written records under FOIA. At CTP, product applications, reports, and correspondence with manufacturers,...
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Question and Answer with Ann Simoneau, Director of CTP’s Office of Compliance and...

Question and Answer with Ann Simoneau, Director of CTP’s Office of Compliance and Enforcement
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FDA Authorizes Modified Risk Tobacco Products

On October 22, 2019, FDA granted the first-ever modified risk orders to Swedish Match USA, Inc. for eight snus smokeless tobacco products. This means the eight products may be advertised with specific information about the lower risks of certain...
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FDA Software Helps Tobacco Product Manufacturers Meet FDA’s Compliance Deadlines

When FDA expanded its authority to regulate all tobacco products in 2016, products including but not limited to electronic nicotine delivery systems (ENDS), cigars, hookah and pipe tobacco were deemed subject to FDA regulation. Thus, manufacturers...
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Upcoming Tobacco Product Listing Deadline — June 30: What Does the Deadline Mean to...

A deadline is approaching for certain manufacturers of deemed tobacco products to provide a listing of their tobacco products to FDA. The agency has undertaken efforts to educate those who could be affected by answering questions such as: What is...
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Marketing ENDS as New Tobacco Products: A Guide for Manufacturers

Applying to legally market a tobacco product in compliance with FDA regulations may feel complicated and confusing, especially for first time applicants. While there are three main ways to bring a new tobacco product to market, a premarket tobacco...
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CTP’s Office of Small Business Assistance

Need help understanding and complying with FDA's tobacco laws and regulations?
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Question and Answer with Matt Holman, Ph.D., Director of CTP’s Office of Science

Matt Holman, Ph.D., Director of the FDA’s Center for Tobacco Products’ (CTP) Office of Science, has over 17 years of experience working as a regulatory scientist, getting his start at FDA in the Center for Drug Evaluation and Research (CDER)....
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How Could Lowering Nicotine Levels in Cigarettes Change the Future of Public Health?

On March 15, 2018, FDA issued an advance notice of proposed rulemaking (ANPRM) to seek comments on a potential nicotine product standard, encouraging the public to submit comments, research, and data on a number of related topics.
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