98-11742. Dental Plaque Subcommittee of the Nonprescription Drugs Advisory Committee; Notice of Meeting  

  • [Federal Register Volume 63, Number 85 (Monday, May 4, 1998)]
    [Notices]
    [Pages 24558-24559]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 98-11742]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    
    
    Dental Plaque Subcommittee of the Nonprescription Drugs Advisory 
    Committee; Notice of Meeting
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Notice.
    
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        This notice announces a forthcoming meeting of a public advisory 
    committee of the Food and Drug Administration (FDA). The meeting will 
    be open to the public.
        Name of Committee: Dental Plaque Subcommittee of the 
    Nonprescription Drugs Advisory Committee.
        General Function of the Committee: To provide advice and 
    recommendations to the agency on FDA's regulatory issues.
        Date and Time: The meeting will be held on May 27, 28, and 29, 
    1998, 8:30 a.m. to 5 p.m.
        Location: Holiday Inn, Two Montgomery Village Ave., Gaithersburg, 
    MD.
        Contact Person: Robert L. Sherman or Stephanie A. Mason, Center for 
    Drug Evaluation and Research (HFD-560), Food and Drug Administration, 
    5600 Fishers Lane, Rockville, MD, 301-827-5191, or FDA Advisory 
    Committee Information Line, 1-800-741-8138 (301-443-0572 in the 
    Washington, DC area), code 12541. Please call the Information Line for 
    up-to-date information on this meeting.
        Agenda: On May 27, 1998, the subcommittee will discuss: (1) The 
    safety and effectiveness of the combination of stannous pyrophosphate 
    and zinc citrate; (2) the effectiveness of the combination of hydrogen 
    peroxide, sodium lauryl sulfate, sodium citrate and zinc chloride; (3) 
    the safety and effectiveness of hexetidine, soluble pyrophosphate, 
    nonsaponifiable fraction of corn oil, bromchlorophene and chlorhexidine 
    digluconate; and (4) final formulation testing. On May 28, 1998, the 
    subcommittee will discuss labeling
    
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    of over-the-counter antiplaque-antigingivitis drug products. On May 29, 
    1998, the subcommittee will discuss recommended therapeutic 
    combinations for antiplaque-antigingivitis drug products.
        Procedure: 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 by May 20, 1998. 
    Oral presentations from the public will be scheduled between 
    approximately 8:30 a.m. and 12 m. on May 27, 28, and 29, 1998. Time 
    allotted for each presentation may be limited. Those desiring to make 
    formal oral presentations should notify the contact person before May 
    20, 1998, 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.
        Notice of this meeting is given under the Federal Advisory 
    Committee Act (5 U.S.C. app. 2).
    
        Dated: April 24, 1998.
    Michael A. Friedman,
    Deputy Commissioner for Operations.
    [FR Doc. 98-11742 Filed 5-1-98; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
05/04/1998
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
98-11742
Pages:
24558-24559 (2 pages)
PDF File:
98-11742.pdf