99-11454. Agency Information Collection Activities; Submission for OMB Review; Comment Request and Correction; Premarket Notification for a New Dietary Ingredient  

  • [Federal Register Volume 64, Number 88 (Friday, May 7, 1999)]
    [Notices]
    [Pages 24660-24661]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 99-11454]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    [Docket No. 99N-0124]
    
    
    Agency Information Collection Activities; Submission for OMB 
    Review; Comment Request and Correction; Premarket Notification for a 
    New Dietary Ingredient
    
    AGENCY: Food and Drug Administration, HHS.
    ACTION: Notice; correction.
    
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    SUMMARY: The Food and Drug Administration (FDA) is announcing that the 
    proposed collection of information listed below has been submitted to 
    the Office of Management and Budget (OMB) for review and clearance 
    under the Paperwork Reduction Act of 1995 (the PRA). In addition, this 
    document is correcting the information collection notice that appeared 
    in the Federal Register of February 9, 1999 (64 FR 6364).
    DATES: Submit written comments on the collection of information by June 
    7, 1999.
    ADDRESSES: Submit written comments on the collection of information to 
    the Office of Information and Regulatory Affairs, OMB, New Executive 
    Office Bldg., 725 17th St. NW., rm. 10235, Washington, DC 20503, Attn: 
    Desk Officer for FDA.
    
    FOR FURTHER INFORMATION CONTACT: Peggy Schlosburg, Office of 
    Information Resources Management (HFA-250), Food and Drug 
    Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-827-1223.
    
    SUPPLEMENTARY INFORMATION: In compliance with section 3507 of the PRA 
    (44 U.S.C. 3507), FDA has submitted the following proposed collection 
    of information to OMB for review and clearance.
    Premarket Notification for a New Dietary Ingredient--21 CFR 190.6 (OMB 
    Control Number 0910-0330--Extension)
        Description: Section 413(a) of the Federal Food, Drug, and Cosmetic 
    Act (the act) (21 U.S.C. 350b(a)) provides for the notification of the 
    Secretary of Health and Human Services (the Secretary) (and by 
    delegation FDA) at least 75 days before the introduction or delivery 
    for introduction into interstate commerce of a dietary supplement that 
    contains a new dietary ingredient. The agency established 21 CFR 190.6 
    as the procedural regulation for this program. This regulation provides 
    details of the administrative procedures associated with the submission 
    and identifies the information that must be included in the submission 
    in order to meet the requirements of section 413(a) of the act and to 
    show the basis on which a manufacturer or distributor of a new dietary 
    ingredient or a dietary supplement containing a new dietary ingredient 
    has concluded that the dietary supplement containing such dietary 
    ingredient will reasonably be expected to be safe.
        Description of Respondents: Businesses or other for-profit 
    organizations.
        In the Federal Register of February 9, 1999 (64 FR 6364), the 
    agency requested comments on the proposed collections of information. 
    No comments were received.
    
                                      Table 1.--Estimated Annual Reporting Burden1
    ----------------------------------------------------------------------------------------------------------------
                                                          Annual
             21 CFR Section               No. of       Frequency per   Total Annual      Hours per      Total Hours
                                        Respondents      Response        Responses       Response
    ----------------------------------------------------------------------------------------------------------------
    190.6                                  11               1              11              20             220
    ----------------------------------------------------------------------------------------------------------------
    \1\ There are no capital costs or operating and maintenance costs associated with this collection of information
    
        The agency believes that there will be a minimal burden on the 
    industry to generate data to meet the requirements of the premarket 
    notification program because the agency is requesting only that 
    information that the manufacturer or distributor should already have 
    developed to satisfy itself that a dietary supplement containing a new 
    dietary ingredient is in full compliance with the act. However, the 
    agency estimates that extracting and summarizing the relevant 
    information from the company's files, and presenting it in a format 
    that will meet the requirements of section 413 of the act, will require 
    a burden of approximately 20 hours of work per submission. This 
    estimate is based on the average number of premarket notifications 
    received by the agency in the last 3 years.
        Additionally, in FR Doc. 99-3014, appearing on page 6364 in the 
    Federal Register of Tuesday, February 9, 1999, the following correction 
    is made:
        1. On page 6365, in the first column, the title ``New Dietary 
    Ingredient Premarket Notification--21 CFR 190.6 (OMB Control Number 
    0910-0330--
    
    [[Page 24661]]
    
    Extension)'' is corrected to read ``Premarket Notification for a New 
    Dietary Ingredient--21 CFR 190.6 (OMB Control Number 0910-0330--
    Extension)''
    
        Dated: April 29, 1999.
    William K. Hubbard,
    Associate Commissioner for Policy Coordination.
    [FR Doc. 99-11454 Filed 5-6-99; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
05/07/1999
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice; correction.
Document Number:
99-11454
Dates:
Submit written comments on the collection of information by June 7, 1999.
Pages:
24660-24661 (2 pages)
Docket Numbers:
Docket No. 99N-0124
PDF File:
99-11454.pdf