98-31030. Closure Medical Corp.; Withdrawal of Color Additive Petition  

  • [Federal Register Volume 63, Number 224 (Friday, November 20, 1998)]
    [Notices]
    [Pages 64512-64513]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 98-31030]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    [Docket No. 97C-0171]
    
    
    Closure Medical Corp.; Withdrawal of Color Additive Petition
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Notice.
    
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    SUMMARY: The Food and Drug Administration (FDA) is announcing the 
    withdrawal, without prejudice to future filing, of a color additive 
    petition (CAP 7C0250) proposing that the color additive regulations be 
    amended to
    
    [[Page 64513]]
    
    provide for the safe use of D&C Violet No. 2 to color 2-octyl 
    cyanoacrylate topical tissue adhesives.
    
    FOR FURTHER INFORMATION CONTACT: Ellen M. Waldron, Center for Food 
    Safety and Applied Nutrition (HFS-215), Food and Drug Administration, 
    200 C St. SW., Washington, DC 20204, 202-418-3089.
    
    SUPPLEMENTARY INFORMATION: In a notice published in the Federal 
    Register of May 1, 1997 (62 FR 23781), FDA announced that a color 
    additive petition (CAP 7C0250) had been filed by Closure Medical Corp., 
    5265 Capital Blvd., Raleigh, NC 27616 (currently 5250 Greens Dairy Rd., 
    Raleigh, NC 27616). The petition proposed to amend the color additive 
    regulations in Sec. 74.3602 D&C Violet No. 2 (21 CFR 74.3602) to 
    provide for the safe use of D&C Violet No. 2 to color 2-octyl 
    cyanoacrylate topical tissue adhesives.
        With the passage of the Medical Device Amendments of 1976 (Pub. L. 
    94-295), Congress mandated the listing of color additives for use in 
    medical devices when the color additive in the device comes into direct 
    contact with the body for a significant period of time (21 U.S.C. 
    379e(a)). Since the filing of this petition, the agency has determined 
    that the proposed use of the subject topical tissue adhesives, and 
    therefore, any color additive used in these adhesives, would not 
    contact the body for a significant period of time (Ref. 1). 
    Consequently, the petitioned use of D&C Violet No. 2 is exempt from the 
    statutory listing requirement. Therefore, Closure Medical Corp. has now 
    withdrawn the petition without prejudice to a future filing (21 CFR 
    71.6(c)(2)) (Ref. 2).
        The agency received two comments on the safety of D&C Violet No. 2 
    in response to the notice of filing for this petition. Arts, Crafts & 
    Theater Safety, Inc. (ACTS) commented that D&C Violet No. 2 could 
    possibly be a carcinogen, based on studies of other anthraquinone dyes 
    and structurally related compounds that concluded those substances were 
    reasonably anticipated to be human carcinogens. They stated that the 
    petition should be denied unless D&C Violet No. 2 is studied for cancer 
    effects and found to show no evidence of carcinogenicity. In response 
    to ACTS'' comment, Flamm Associates commented that in addition to a 
    consideration of the general chemical class of a substance, other 
    structural features need to be evaluated in determining the 
    carcinogenic potential of a substance. They further stated that D&C 
    Violet No. 2 has been tested for carcinogenicity and found to be 
    noncarcinogenic.
        The agency concludes that, although the subject petition is being 
    withdrawn, the safety of the currently approved uses of D&C Violet No. 
    2 (21 CFR 74.1602, 74.2602 and 74.3602) is supported by an extensive 
    body of toxicity testing data and that the comments provide no basis 
    for a safety concern.
    
    References
    
        The following references have been placed on display in the Dockets 
    Management Branch (HFA-305), 5630 Fishers Lane, Rockville, MD 20852 and 
    may be seen by interested persons between 9 a.m. and 4 p.m., Monday 
    through Friday.
        1. Memorandum from Office of Device Evaluation, Program 
    Operations Staff (Center for Devices and Radiological Health, FDA), 
    to Division of Petition Control (Center for Food Safety and Applied 
    Nutrition, FDA), concerning ``CAP 7C0250'', dated October 23, 1998.
        2. Letter from Hyman, Phelps & McNamara, P.C., to Office of 
    Premarket Approval (FDA), dated August 25, 1998.
    
        Dated: November 3, 1998.
    Laura M. Tarantino,
    Acting Director, Office of Premarket Approval, Center for Food Safety 
    and Applied Nutrition.
    [FR Doc. 98-31030 Filed 11-19-98; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
11/20/1998
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
98-31030
Pages:
64512-64513 (2 pages)
Docket Numbers:
Docket No. 97C-0171
PDF File:
98-31030.pdf