International Pharmaceutical Transparency Act of 2019
This bill prohibits the sale of a drug if its label fails to list the country of origin of each of the drug's active ingredients.
[Congressional Bills 116th Congress]
[From the U.S. Government Publishing Office]
[H.R. 5381 Introduced in House (IH)]
<DOC>
116th CONGRESS
1st Session
H. R. 5381
To amend the Federal Food, Drug, and Cosmetic Act to require the label
of a drug to list the country of origin of each of the drug's active
ingredients.
_______________________________________________________________________
IN THE HOUSE OF REPRESENTATIVES
December 10, 2019
Mr. DesJarlais 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 require the label
of a drug to list the country of origin of each of the drug's active
ingredients.
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 ``International Pharmaceutical
Transparency Act of 2019''.
SEC. 2. COUNTRY-OF-ORIGIN LABELING FOR ACTIVE INGREDIENTS IN DRUGS.
(a) Misbranding.--Section 502 of the Federal Food, Drug, and
Cosmetic Act (21 U.S.C. 352) is amended by adding at the end the
following:
``(ee) If it is a drug and its label fails to list the country of
origin of each of its active ingredients.''.
(b) Applicability.--Section 502(ee) of the Federal Food, Drug, and
Cosmetic Act, as added by subsection (a), applies beginning on the day
that is 6 months after the date of enactment of this Act.
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Introduced in House
Introduced in House
Referred to the House Committee on Energy and Commerce.
Referred to the Subcommittee on Health.
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