tocacco plant Native American Tobaccoo flower, leaves, and buds

tocacco Tobacco is an annual or bi-annual growing 1-3 meters tall with large sticky leaves that contain nicotine. Native to the Americas, tobacco has a long history of use as a shamanic inebriant and stimulant. It is extremely popular and well-known for its addictive potential.

tocacco nicotina Nicotiana tabacum

tocacco Nicotiana rustica leaves. Nicotiana rustica leaves have a nicotine content as high as 9%, whereas Nicotiana tabacum (common tobacco) leaves contain about 1 to 3%

tocacco cigar A cigar is a tightly rolled bundle of dried and fermented tobacco which is ignited so that its smoke may be drawn into the mouth. Cigar tobacco is grown in significant quantities in Brazil, Cameroon, Cuba, Dominican Republic, Honduras, Indonesia, Mexico, Nicaragua, Sumatra, Philippines, and the Eastern United States.

tocacco Tobacco is an agricultural product processed from the fresh leaves of plants in the genus Nicotiana. It can be consumed, used as an organic pesticide, and in the form of nicotine tartrate it is used in some medicines. In consumption it may be in the form of cigarettes smoking, snuffing, chewing, dipping tobacco, or snus.

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July 15-16 Meeting of the Tobacco Products Scientific Advisory Committee

July 15, 2010
& July 16, 2010

8:30 a.m. – 5:00 p.m.
8:00 a.m. - 5:00 p.m.

Gaithersburg Marriott Washingtonian Center
9751 Washingtonian Boulevard
Gaithersburg, Maryland
Hotel phone number is 301-590-0044.


On July 15, 2010, the committee will 1) hear and discuss a presentation on dissolvable tobacco products in order to prepare for the Tobacco Products Scientific Advisory Committee’s required report to the Secretary of Health and Human Services regarding the impact of the use of dissolvable tobacco products on the public health, 2) receive updates on upcoming committee business related to menthol, including Agency requests for information from industry on menthol cigarettes in order to prepare for the Tobacco Products Scientific Advisory Committee’s required report to the Secretary of Health and Human Services regarding the impact of use of menthol in cigarettes on the public health, and 3) hear and discuss industry presentations on menthol in cigarettes as they relate to five topics: characterization of menthol, clinical effects of menthol, biomarkers of disease risk, marketing data, and population effects. Specific areas of interest identified by the committee for industry presentations include:
Characterization of menthol
1) Trends in quantities of menthol present in the cigarette rod and smoke over time for various brands/subbrands of menthol and nonmenthol products as determined by the Cambridge Filter/ISO test method using standard parameters as well as the intense smoking conditions set forth in Canadian regulations.
2) Information regarding the manufacturing of menthol and nonmenthol cigarettes, including a) the source and type of menthol used, b) the presence or use of any menthol analogs, and c) the types of manufacturing processes through which menthol is introduced into the tobacco product, as well as the considerations in selecting a particular method.
3) The threshold (menthol content) at which a product is identified and marketed as a menthol cigarette and how that threshold is established.
4) The rationale for adding menthol to cigarettes not marketed as menthol cigarettes, and the criteria for determining the quantity of menthol to be added.
5) For international brands of menthol cigarettes, the quantities of menthol in both menthol and nonmenthol cigarettes sold internationally, and the factors considered in determining the quantity of menthol to be added.
Clinical effects of menthol
6) Studies of dose-response relationships for the physiologic effects of mentholated tobacco smoke.
7) Mechanistic studies of menthol effects including, a) chemosensory effects of menthol compounds in tobacco smoke, including effects at thermal and trigeminal receptors, b) the effect of menthol on the neurobiology of tobacco dependence, and c) the effect of menthol on clinical and behavioral measures.
8) Studies addressing the dosing relationship and the metabolic interactions between nicotine and menthol, including resulting perceptions of nicotine strength and the interaction between menthol delivery and nicotine/tar levels, for both low-menthol and high-menthol products.
9) Information on correlations between menthol content and consumer perceptions
regarding a) taste, b) nicotine strength, and c) product harm.
10) Analyses of laboratory and populations studies using biomarkers to assess the effect of menthol content on disease risk for cigarette smokers, based on cigarette consumption (e.g., cigarettes per day), including data related to menthol among population subgroups.
Marketing data
11) Data on consumer preferences for menthol cigarettes.
12) Consumer perception studies of advertising, packaging, and labeling of menthol cigarettes.
13) Marketing strategies for various brands/subbrands of menthol cigarettes, including strategies targeted to particular demographic groups.
14) Marketing strategies for various brands/subbrands of menthol cigarettes sold internationally.
Population effects
15) Among cigarette smokers, rates of switching from menthol to nonmenthol cigarettes and vice versa.
16) Comparative rates of initiation by youth and young adults with menthol and nonmenthol cigarettes.
17) Comparative rates of cessation for users of menthol and nonmenthol cigarettes.

Information regarding menthol derived from both natural and synthetic sources, as well as menthol analogs and functional equivalents will be important to the committee in evaluating the impact of the use of menthol in cigarettes on the public health. Furthermore, FDA asks that to the extent possible and where relevant, data prepared for the presentations be stratified by gender, race/ethnicity, and age.
On July 16, 2010, the committee will continue discussion on topic 3.

The FDA will work with representatives of the tobacco industry who wish to make presentations to ensure that adequate time, separate from the time slots for the general Open Public Hearing, is provided. Companies interested in making formal presentations to the Committee should respond by June 10, 2010, to [email protected] with the following: 1) confirmation of your availability to present at the July 15-16, 2010 TPSAC meeting, 2) specific topics for which you have relevant information and which you intend to present during the July 15-16, 2010 TPSAC meeting, and 3) whether you are planning to provide background materials for the committee before the meeting. Each of the five broad categories listed in the Agenda portion of this notice will be allotted approximately one hour of presentation time during the meeting. Companies with common interest are urged to coordinate their oral presentations.

Meeting Materials

Links to meeting materials will be added as they become available.
Public Participation Information

Interested persons may present data, information, or views, orally or in writing, on issues pending before the committee.

  • Written submissions may be made to the contact person on or before
    June 30, 2010.
  • Oral presentations from the public will be scheduled between approximately
    9:00 and 9:15 a.m. on July 15, 2010 for dissolvable tobacco products, and 12:30 and 1:30 p.m. on July 16, 2010 for menthol. Those desiring to make formal oral
    presentations should notify the contact person and submit a brief statement of the
    general nature of the evidence or arguments they wish to present, the names and
    addresses of proposed participants, and an indication of the approximate time
    requested to make their presentation on or before June 21, 2010.

    Time allotted for each presentation may be limited. If the number of registrants requesting to speak is greater than can be reasonably accommodated during the scheduled open public hearing session, FDA may conduct a lottery to determine the speakers for the scheduled open public hearing session. The contact person will notify interested persons regarding their request to speak by June 23, 2010.

Contact Information

  • Cristi Stark, M.S.
    Center for Tobacco Products
    Food and Drug Administration
    9200 Corporate Boulevard
    Rockville, MD 20850

    Phone: 1-877-287-1373 (choose Option 4)
    FAX: 240-276-3904
    Email: [email protected]

  • FDA Advisory Committee Information Line
    (301-443-0572 in the Washington DC area)
    Code: 8732110002
    Please call the Information Line for up-to-date information on this meeting.

A notice in the Federal Register about last minute modifications that impact a previously announced advisory committee meeting cannot always be published quickly enough to provide timely notice. Therefore, you should always check the agency’s Website and call the appropriate advisory committee hot line/phone line to learn about possible modifications before coming to the meeting.

FDA intends to make background material available to the public no later than 2 business days before the meeting. If FDA is unable to post the background material on its Web site prior to the meeting, the background material will be made publicly available at the location of the advisory committee meeting, and the background material will be posted on FDA’s Web site after the meeting.

Persons attending FDA’s advisory committee meetings are advised that the agency is not responsible for providing access to electrical outlets. FDA welcomes the attendance of the public at its advisory committee meetings and will make every effort to accommodate persons with physical disabilities or special needs. If you require special accommodations due to a disability, please contact Cristi Stark at 1-877-287-1373 (choose Option 4) or [email protected] at least 7 days in advance of the meeting.

FDA is committed to the orderly conduct of its advisory committee meetings. Please visit our Web site at for procedures on public conduct during advisory committee meetings.

Notice of this meeting is given under the Federal Advisory Committee Act (5 U.S.C. app.2).

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