Bill Sponsor
House Bill 421
115th Congress(2017-2018)
Allowing Greater Access to Safe and Effective Contraception Act
Introduced
Introduced
Introduced in House on Jan 10, 2017
Overview
Text
Introduced in House 
Jan 10, 2017
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Introduced in House(Jan 10, 2017)
Jan 10, 2017
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Multiple bills can contain the same text. This could be an identical bill in the opposite chamber or a smaller bill with a section embedded in a larger bill.
Bill Sponsor regularly scans bill texts to find sections that are contained in other bill texts. When a matching section is found, the bills containing that section can be viewed by clicking "View Bills" within the bill text section.
Bill Sponsor is currently only finding exact word-for-word section matches. In a future release, partial matches will be included.
H. R. 421 (Introduced-in-House)


115th CONGRESS
1st Session
H. R. 421


To allow women greater access to safe and effective contraception.


IN THE HOUSE OF REPRESENTATIVES

January 10, 2017

Mrs. Love (for herself, Mrs. Comstock, Mr. Stewart, Mr. Coffman, and Mr. Kinzinger) introduced the following bill; which was referred to the Committee on Ways and Means, and in addition to the Committee on Energy and Commerce, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned


A BILL

To allow women greater access to safe and effective contraception.

Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled,

SECTION 1. Short title.

This Act may be cited as the “Allowing Greater Access to Safe and Effective Contraception Act”.

SEC. 2. Applications for non-prescription contraceptive drugs.

(a) Priority review of application.—The Secretary of Health and Human Services (referred to in this section as the “Secretary”) shall give priority review to any supplemental application submitted under section 505(b) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355(b)) for a contraceptive drug, provided that—

(1) the supplemental application is with respect to a drug intended for routine use; and

(2) if the supplemental application is approved, with respect to individuals aged 18 and older, such drug would not be subject to section 503(b)(1) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 353(b)(1)).

(b) Fee waiver.—The Secretary shall waive the fee under section 736(a)(1) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 379h(a)(1)) with respect to a supplemental application that receives priority review under subsection (a).

(c) Over-the-Counter availability.—Notwithstanding any other provision of law, with respect to individuals under age 18, a contraceptive drug that is eligible for priority review under subsection (a) shall be subject to section 503(b)(1) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 353(b)(1)).

SEC. 3. Empowering women to make their own health decisions.

(a) No limitations based on whether a drug is prescribed.—Section 9003 of the Patient Protection and Affordable Care Act (Public Law 111–148), and the amendments made by such section, are repealed, and the Internal Revenue Code of 1986 shall be applied as if such section, and amendments, had never been enacted.

(b) No limitations on health FSAs.—Sections 9005 and 10902 of the Patient Protection and Affordable Care Act (Public Law 111–148) and section 1403 of the Health Care and Education Reconciliation Act of 2010 (Public Law 111–152), and the amendments made by such sections, are repealed, and the Internal Revenue Code of 1986 shall be applied as if such sections, and amendments, had never been enacted.