U.S. CODE
Rulings
AD/CVD
Notices
HTSUS
U.S. Code
Regs
More
Ports
About
Updates
Apps
Larger font
Smaller font
CustomsMobile Pro
beta now open!
Apply for a FREE beta account. Spaces are limited so apply today.
SIGNUP FOR BETA
SEARCH
Toggle Dropdown
Search US Code
Search Leg. Notes
Sort by Rank
Titles Ascending
Titles Descending
10 per page
25 Result/page
50 Result/page
U.S Code last checked for updates: Nov 22, 2024
All Titles
Title 21
Chapter 9
Subchapter V
Part I
Part H - Pharmaceutical Distribu...
§ 360fff-1. Submission of reques...
Part H - Pharmaceutical Distribu...
§ 360fff-1. Submission of reques...
U.S. Code
Notes
§ 360fff.
Definitions
In this part—
(1)
the term “Advisory Committee” means the Nonprescription Drug Advisory Committee of the Food and Drug Administration or any successor to such Committee;
(2)
the term “final sunscreen order” means an order published by the Secretary in the Federal Register containing information stating that a nonprescription sunscreen active ingredient or combination of nonprescription sunscreen active ingredients—
(A)
is GRASE and is not misbranded if marketed in accordance with such order; or
(B)
is not GRASE and is misbranded;
(3)
the term “GRASE” means generally recognized, among experts qualified by scientific training and experience to evaluate the safety and effectiveness of drugs, as safe and effective for use under the conditions prescribed, recommended, or suggested in the labeling of a drug as described in
section 321(p) of this title
;
(4)
the term “GRASE determination” means, with respect to a nonprescription active ingredient or a combination of nonprescription active ingredients, a determination of whether such ingredient or combination of ingredients is GRASE;
(5)
the term “nonprescription” means not subject to
section 353(b)(1) of this title
;
(6)
the term “pending request” means each request with respect to a nonprescription sunscreen active ingredient submitted under section 330.14 of title 21, Code of Federal Regulations (as in effect on
November 26, 2014
) for consideration for inclusion in the over-the-counter drug monograph system—
(A)
that was determined to be eligible for such review by publication of a notice of eligibility in the Federal Register prior to
November 26, 2014
; and
(B)
for which safety and effectiveness data have been submitted to the Secretary prior to
November 26, 2014
;
(7)
the term “proposed sunscreen order” means an order containing a tentative determination published by the Secretary in the Federal Register containing information proposing that a nonprescription sunscreen active ingredient or combination of nonprescription sunscreen active ingredients—
(A)
is GRASE and is not misbranded if marketed in accordance with such order;
(B)
is not GRASE and is misbranded; or
(C)
is not GRASE and is misbranded because the data are insufficient to classify such ingredient or combination of ingredients as GRASE and not misbranded and additional information is necessary to allow the Secretary to determine otherwise;
(8)
the term “sponsor” means the person that submitted—
(A)
a request under
section 360fff–1 of this title
;
(B)
a pending request; or
(C)
any other application subject to this part;
(9)
the term “sunscreen” means a drug containing one or more sunscreen active ingredients; and
(10)
the term “sunscreen active ingredient” means an active ingredient that is intended for application to the skin of humans for purposes of absorbing, reflecting, or scattering ultraviolet radiation.
(
June 25, 1938, ch. 675, § 586
, as added
Pub. L. 113–195, § 2(a)
,
Nov. 26, 2014
,
128 Stat. 2035
.)
cite as:
21 USC 360fff
.list_box li,p,.cm-search-info,.cm-search-detail,.abt span,.expand-collapse_top
Get the CustomsMobile app!