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I
116TH CONGRESS
1ST SESSION H. R. 2268
To amend the Federal Food, Drug, and Cosmetic Act to treat certain men-
strual products as misbranded if their labeling does not list each ingre-
dient or component of the product, and for other purposes.
IN THE HOUSE OF REPRESENTATIVES
APRIL 10, 2019
Ms. MENG introduced the following bill; which was referred to the Committee
on Energy and Commerce
A BILL
To amend the Federal Food, Drug, and Cosmetic Act to
treat certain menstrual products as misbranded if their
labeling does not list each ingredient or component of
the product, and for other purposes.
Be it enacted by the Senate and House of Representa-
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tives of the United States of America in Congress assembled,
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SECTION 1. SHORT TITLE.
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This Act may be cited as the ‘‘Menstrual Products
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Right To Know Act of 2019’’.
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•HR 2268 IH
SEC. 2. CERTAIN MENSTRUAL PRODUCTS MISBRANDED IF
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LABELING DOES NOT INCLUDE INGREDI-
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ENTS.
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(a) IN GENERAL.—Section 502 of the Federal Food,
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Drug, and Cosmetic Act (21 U.S.C. 352) is amended by
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adding at the end the following:
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‘‘(ee) If it is a menstrual product, such as a men-
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strual cup, a scented, scented deodorized, or unscented
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menstrual pad or tampon, a therapeutic vaginal douche
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apparatus, or an obstetrical and gynecological device de-
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scribed in section 884.5400, 884.5425, 884.5435,
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884.5460, 884.5470, or 884.5900 of title 21, Code of Fed-
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eral Regulations (or any successor regulation), unless its
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label or labeling lists the name of each ingredient or com-
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ponent of the product in order of the most predominant
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ingredient or component to the least predominant ingre-
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dient or component.’’.
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(b) EFFECTIVE DATE.—The amendment made by
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subsection (a) applies with respect to products introduced
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or delivered for introduction into interstate commerce on
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or after the date that is one year after the date of the
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enactment of this Act.
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Æ
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