Impact of Dissolvable Tobacco Use on Public Health; Request for Comments, 13556-13557 [2010-6216]

Download as PDF 13556 Federal Register / Vol. 75, No. 54 / Monday, March 22, 2010 / Notices Fishery Products — Decomposition, which is available on the Internet at https://www.fda.gov/ICECI/Compliance Manuals/CompliancePolicyGuidance Manual/ucm123201.htm. cumulatively have a significant effect on the human environment. Therefore, neither an environmental assessment nor an environmental impact statement is required. Dated: March 9, 2010. Michael A. Chappell, Acting Associate Commissioner for Regulatory Affairs. [FR Doc. 2010–6209 Filed 3–19–10; 8:45 am] Dated: March 5, 2010. Mitchell A. Cheeseman, Acting Director, Office of Food Additive Safety, Center for Food Safety and Applied Nutrition. BILLING CODE 4160–01–S [FR Doc. 2010–6177 Filed 3–19–10; 8:45 am] BILLING CODE 4160–01–S DEPARTMENT OF HEALTH AND HUMAN SERVICES DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Food and Drug Administration [Docket No. FDA–2010–C–0077] [Docket No. FDA–2010–N–0123] Biocompatibles UK Ltd.; Filing of Color Additive Petition AGENCY: Food and Drug Administration, HHS. ACTION: ACTION: The Food and Drug Administration (FDA) is announcing that Biocompatibles UK Ltd., has filed a petition proposing that the color additive regulations be amended to provide for the safe use of C.I. Reactive Blue No. 4 [2-anthracenesulfonic acid, 1-amino-4-(3-((4,6-dichloro-s-triazin-2yl)amino)-4-sulfoanilino)-9,10-dihydro9,10-dioxo, disodium salt] (CAS Reg. No. 4499–01–8) reacted with polyvinyl alcohol as a color additive in vascular embolization devices. FOR FURTHER INFORMATION CONTACT: Judith Kidwell, Center for Food Safety and Applied Nutrition (HFS–265), Food and Drug Administration, 5100 Paint Branch Pkwy., College Park, MD 20740– 3835, 301–436–1071. SUPPLEMENTARY INFORMATION: Under the Federal Food, Drug, and Cosmetic Act (sec. 721(d)(1) (21 U.S.C. 379e(d)(1))), notice is given that a color additive petition (CAP 0C0288) has been filed by Biocompatibles UK Ltd., c/o John Greenbaum, Generic Devices Consulting, Inc., 20310 SW. 48th St, Southwest Ranches, FL 33332. The petition proposes to amend the color additive regulations in 21 CFR part 73, subpart D, Medical Devices, to provide for the safe use of C.I. Reactive Blue No. 4 [2-anthracenesulfonic acid, 1-amino-4(3-((4,6-dichloro-s-triazin-2-yl)amino)-4sulfoanilino)-9,10-dihydro-9,10-dioxo, disodium salt] (CAS Reg. No. 4499–01– 8) reacted with polyvinyl alcohol as a color additive in vascular embolization devices. The agency has determined under 21 CFR 25.32(l) that this action is of a type that does not individually or pwalker on DSK8KYBLC1PROD with NOTICES SUMMARY: 16:41 Mar 19, 2010 AGENCY: Food and Drug Administration, HHS. Notice. VerDate Nov<24>2008 Impact of Dissolvable Tobacco Use on Public Health; Request for Comments Jkt 220001 Notice; request for comments. SUMMARY: The Food and Drug Administration (FDA) is establishing a public docket to provide an opportunity for interested parties to share information, research, and ideas on how use of dissolvable tobacco products may impact public health, including such use among children. This information will be used to support the work of the Tobacco Products Scientific Advisory Committee, which is charged with evaluating this issue. DATES: Submit written or electronic comments by [insert date 180 days from date of publication in the Federal Register]. Submit electronic comments to https:// www.regulations.gov/. Submit written comments to the Division of Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. FOR FURTHER INFORMATION CONTACT: Kathleen K. Quinn, Center for Tobacco Products, Food and Drug Administration, 9200 Corporate Blvd., Rockville, MD 20850–3229, 240–276– 1717, Kathleen.Quinn@fda.hhs.gov. SUPPLEMENTARY INFORMATION: ADDRESSES: I. Background Tobacco products are responsible for more than 440,000 deaths each year. The Centers for Disease Control and Prevention report that every day in the United States, approximately 3,900 young people between these ages of 12 and 17 smoke their first cigarette and approximately 1,000 adolescents become daily smokers. Multiple studies PO 00000 Frm 00074 Fmt 4703 Sfmt 4703 have shown that adolescents who use smokeless tobacco products are more likely to become smokers than those who do not. Dissolvable tobacco products are a novel class of smokeless tobacco products, which are sold as thin strips, tablets, and sticks resembling toothpicks. Because some of these products look like candy, are highly flavored, and can be easily concealed, public health officials have raised concerns that dissolvable tobacco products may be particularly appealing to children and adolescents. These products also contain up to 4.0 milligrams of nicotine per unit, which could facilitate initiation of tobacco use and the development of nicotine dependence in adolescents, or even serve as a mechanism for inadvertent toxicity in children. On June 22, 2009, the President signed the Family Smoking Prevention and Tobacco Control Act (the Tobacco Control Act) into law. The Tobacco Control Act granted FDA important new authority to regulate the manufacture, marketing, and distribution of tobacco products to protect the public health generally and to reduce tobacco use by minors. Among its many provisions, the Tobacco Control Act added section 907(f) to the Federal Food, Drug, and Cosmetic Act (the act). This section requires FDA to refer the issue of ‘‘the nature and impact of the use of dissolvable tobacco products on the public health, including such use among children’’ to a Tobacco Products Scientific Advisory Committee, which will be charged with providing FDA a report and recommendations. We are requesting comments that will support the work of the Tobacco Products Scientific Advisory Committee in evaluating the public health impact of dissolvable tobacco products. A copy of the Tobacco Control Act is available at https://www.fda.gov/tobacco. II. Request for Comments and Information Data around the nature, impact, and use of dissolvables tobacco products will be critical to the Tobacco Products Scientific Advisory Committee in studying and reporting on their public health impact. We are therefore requesting comment, research, and data on ways in which these products might be used by individuals, including children and adolescents, how the risks of using these products are perceived by smokers and non-smokers, and how use of these products affects health. Such research may address: E:\FR\FM\22MRN1.SGM 22MRN1 Federal Register / Vol. 75, No. 54 / Monday, March 22, 2010 / Notices • Perceptions of dissolvable tobacco products from current tobacco users and ¨ tobacco-naıve individuals, by age; • Marketing of dissolvable tobacco products to current tobacco users and ¨ tobacco-naıve individuals, by age; • Impact of dissolvable tobacco products on initiation of tobacco use in ¨ tobacco-naıve individuals, by age; • Dual use of dissolvable tobacco products by current tobacco users; • Impact of dissolvable tobacco products on cessation of tobacco use; • Risk of accidental ingestion of dissolvable tobacco products; • Risk of accidental nicotine toxicity through use of dissolvable tobacco products; and • Consumer understanding of the potential toxicity of dissolvable tobacco products to children. III. Comments Interested persons may submit to the Division of Dockets Management (see ADDRESSES) written or electronic comments regarding this document. Submit a single copy of electronic comments or two paper copies of any mailed comments, except that individuals may submit one paper copy. Comments are to be identified by the docket number found in brackets in the heading of this document. Received comments may be seen in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday. Dated: March 17, 2010. Leslie Kux, Acting Assistant Commissioner for Policy. Name of Committee: Center for Scientific Review Special Emphasis Panel, Member Conflict: Molecular and Cellular Neuroscience. Date: April 1, 2010. Time: 1 p.m. to 4 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD 20892. (Telephone Conference Call.) Contact Person: Laurent Taupenot, PhD, Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 4811, MSC 7850, Bethesda, MD 20892. 301–435– 1203. taupenol@csr.nih.gov. This notice is being published less than 15 days prior to the meeting due to the timing limitations imposed by the review and funding cycle. Name of Committee: Center for Scientific Review Special Emphasis Panel, Member Conflict: Virology and Viral Immunity. Date: April 6–7, 2010. Time: 8 a.m. to 5 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD 20892. (Virtual Meeting). Contact Person: Richard G. Kostriken, PhD, Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 3192, MSC 7808, Bethesda, MD 20892. 301–402– 4454. kostrikr@csr.nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.306, Comparative Medicine; 93.333, Clinical Research, 93.306, 93.333, 93.337, 93.393–93.396, 93.837–93.844, 93.846–93.878, 93.892, 93.893, National Institutes of Health, HHS) Dated: March 15, 2010. Jennifer Spaeth, Director, Office of Federal Advisory Committee Policy. [FR Doc. 2010–6216 Filed 3–19–10; 8:45 am] BILLING CODE 4160–01–S [FR Doc. 2010–6107 Filed 3–19–10; 8:45 am] DEPARTMENT OF HEALTH AND HUMAN SERVICES BILLING CODE 4140–01–P National Institutes of Health pwalker on DSK8KYBLC1PROD with NOTICES Center for Scientific Review; Notice of Closed Meetings Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of the following meetings. The meetings will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. VerDate Nov<24>2008 16:41 Mar 19, 2010 Jkt 220001 DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute of General Medical Sciences; Notice of Closed Meeting Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant PO 00000 Frm 00075 Fmt 4703 Sfmt 4703 13557 applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Institute of General Medical Sciences Special Emphasis Panel; Eureka Meeting. Date: April 15–16, 2010. Time: 8 a.m. to 5 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, Natcher Building, 45 Center Drive, Room 3AN12B, Bethesda, MD 20892, (Virtual Meeting). Contact Person: Lisa A. Dunbar, PhD, Scientific Review Officer, Office of Scientific Review, National Institute of General Medical Sciences, National Institutes of Health, 45 Center Drive, Room 3AN12, Bethesda, MD 20892, 301–594–2849, dunbarl@mail.nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.375, Minority Biomedical Research Support; 93.821, Cell Biology and Biophysics Research; 93.859, Pharmacology, Physiology, and Biological Chemistry Research; 93.862, Genetics and Developmental Biology Research; 93.88, Minority Access to Research Careers; 93.96, Special Minority Initiatives, National Institutes of Health, HHS) Dated: March 12, 2010. Jennifer Spaeth, Director, Office of Federal Advisory Committee Policy. [FR Doc. 2010–6112 Filed 3–19–10; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute of Diabetes and Digestive and Kidney Diseases; Notice of Closed Meeting Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Institute of Diabetes and Digestive and Kidney Diseases Special Emphasis Panel, LRP Reviews. Date: May 7, 2010. Time: 2 p.m. to 4 p.m. Agenda: To review and evaluate grant applications. E:\FR\FM\22MRN1.SGM 22MRN1

Agencies

[Federal Register Volume 75, Number 54 (Monday, March 22, 2010)]
[Notices]
[Pages 13556-13557]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-6216]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2010-N-0123]


Impact of Dissolvable Tobacco Use on Public Health; Request for 
Comments

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice; request for comments.

-----------------------------------------------------------------------

SUMMARY: The Food and Drug Administration (FDA) is establishing a 
public docket to provide an opportunity for interested parties to share 
information, research, and ideas on how use of dissolvable tobacco 
products may impact public health, including such use among children. 
This information will be used to support the work of the Tobacco 
Products Scientific Advisory Committee, which is charged with 
evaluating this issue.

DATES: Submit written or electronic comments by [insert date 180 days 
from date of publication in the Federal Register].

ADDRESSES: Submit electronic comments to https://www.regulations.gov/. 
Submit written comments to the Division of Dockets Management (HFA-
305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, 
Rockville, MD 20852.

FOR FURTHER INFORMATION CONTACT: Kathleen K. Quinn, Center for Tobacco 
Products, Food and Drug Administration, 9200 Corporate Blvd., 
Rockville, MD 20850-3229, 240-276-1717, Kathleen.Quinn@fda.hhs.gov.

SUPPLEMENTARY INFORMATION:

I. Background

    Tobacco products are responsible for more than 440,000 deaths each 
year. The Centers for Disease Control and Prevention report that every 
day in the United States, approximately 3,900 young people between 
these ages of 12 and 17 smoke their first cigarette and approximately 
1,000 adolescents become daily smokers. Multiple studies have shown 
that adolescents who use smokeless tobacco products are more likely to 
become smokers than those who do not.
    Dissolvable tobacco products are a novel class of smokeless tobacco 
products, which are sold as thin strips, tablets, and sticks resembling 
toothpicks. Because some of these products look like candy, are highly 
flavored, and can be easily concealed, public health officials have 
raised concerns that dissolvable tobacco products may be particularly 
appealing to children and adolescents. These products also contain up 
to 4.0 milligrams of nicotine per unit, which could facilitate 
initiation of tobacco use and the development of nicotine dependence in 
adolescents, or even serve as a mechanism for inadvertent toxicity in 
children.
    On June 22, 2009, the President signed the Family Smoking 
Prevention and Tobacco Control Act (the Tobacco Control Act) into law. 
The Tobacco Control Act granted FDA important new authority to regulate 
the manufacture, marketing, and distribution of tobacco products to 
protect the public health generally and to reduce tobacco use by 
minors. Among its many provisions, the Tobacco Control Act added 
section 907(f) to the Federal Food, Drug, and Cosmetic Act (the act). 
This section requires FDA to refer the issue of ``the nature and impact 
of the use of dissolvable tobacco products on the public health, 
including such use among children'' to a Tobacco Products Scientific 
Advisory Committee, which will be charged with providing FDA a report 
and recommendations.
    We are requesting comments that will support the work of the 
Tobacco Products Scientific Advisory Committee in evaluating the public 
health impact of dissolvable tobacco products. A copy of the Tobacco 
Control Act is available at https://www.fda.gov/tobacco.

II. Request for Comments and Information

    Data around the nature, impact, and use of dissolvables tobacco 
products will be critical to the Tobacco Products Scientific Advisory 
Committee in studying and reporting on their public health impact. We 
are therefore requesting comment, research, and data on ways in which 
these products might be used by individuals, including children and 
adolescents, how the risks of using these products are perceived by 
smokers and non-smokers, and how use of these products affects health. 
Such research may address:

[[Page 13557]]

     Perceptions of dissolvable tobacco products from current 
tobacco users and tobacco-na[iuml]ve individuals, by age;
     Marketing of dissolvable tobacco products to current 
tobacco users and tobacco-na[iuml]ve individuals, by age;
     Impact of dissolvable tobacco products on initiation of 
tobacco use in tobacco-na[iuml]ve individuals, by age;
     Dual use of dissolvable tobacco products by current 
tobacco users;
     Impact of dissolvable tobacco products on cessation of 
tobacco use;
     Risk of accidental ingestion of dissolvable tobacco 
products;
     Risk of accidental nicotine toxicity through use of 
dissolvable tobacco products; and
     Consumer understanding of the potential toxicity of 
dissolvable tobacco products to children.

III. Comments

    Interested persons may submit to the Division of Dockets Management 
(see ADDRESSES) written or electronic comments regarding this document. 
Submit a single copy of electronic comments or two paper copies of any 
mailed comments, except that individuals may submit one paper copy. 
Comments are to be identified by the docket number found in brackets in 
the heading of this document. Received comments may be seen in the 
Division of Dockets Management between 9 a.m. and 4 p.m., Monday 
through Friday.

    Dated: March 17, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010-6216 Filed 3-19-10; 8:45 am]
BILLING CODE 4160-01-S
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