[Federal Register Volume 62, Number 38 (Wednesday, February 26, 1997)]
[Proposed Rules]
[Pages 8663-8664]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 97-4730]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 352

[Docket No. 78N-0038]
RIN 0910-AA01


Sunscreen Drug Products for Over-the-Counter Human Use; Amendment 
to the Tentative Final Monograph; Correction

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice of proposed rulemaking; correction.

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SUMMARY: The Food and Drug Administration (FDA) is correcting a notice 
of proposed rulemaking that appeared in the Federal Register of 
September 16, 1996 (61 FR 48645). The document proposed to amend the 
tentative final monograph (proposed rule) for over-the-counter (OTC) 
sunscreen drug products. The document was published with an error. This 
document corrects that error.


[[Page 8664]]


FOR FURTHER INFORMATION CONTACT: John D. Lipnicki, Center for Drug 
Evaluation and Research (HFD-560), Food and Drug Administration, 5600 
Fishers Lane, Rockville, MD 20857, 301-827-2222.
    In FR Doc. 96-23547, appearing on page 48645 in the Federal 
Register of Monday, September 16, 1996, the following correction is 
made:


Sec. 352.20  [Corrected]

    1. On page 48654, in the third column, in Sec. 352.20 Permitted 
combination of active ingredients, in paragraph (a)(2), beginning in 
the second line, ``Sec. 352.10(b), (c), (f), (i), (k), (l), (m), (n), 
(o), (s), and (u)'' is corrected to read ``Sec. 352.10(b), (c), (d), 
(f), (i), (l), (m), (n), (o), (s), and (u)''.

    Dated: February 19, 1997.
William K. Hubbard,
Associate Commissioner for Policy Coordination.
[FR Doc. 97-4730 Filed 2-25-97; 8:45 am]
BILLING CODE 4160-01-F