H.R. 6190 (112th): Asthma Inhalers Relief Act of 2012

Introduced:
Jul 25, 2012 (112th Congress, 2011–2013)
Sponsor:
Rep. Michael Burgess [R-TX26]
Status:
Died (Failed Under Suspension)
See Instead:
This bill was re-introduced as H.R. 1220 on Mar 15, 2013. See H.R. 1220 for current action on this subject.

The bill’s title was written by the bill’s sponsor. H.R. stands for House of Representatives bill.

GovTrack’s Bill Summary

We don’t have a summary available yet.

Library of Congress Summary

The summary below was written by the Congressional Research Service, which is a nonpartisan division of the Library of Congress.


9/14/2012--Reported to House without amendment.
(This measure has not been amended since it was introduced.
The summary of that version is repeated here.) Asthma Inhalers Relief Act of 2012 - Directs the Administrator of the Environmental Protection Agency (EPA) to:
(1) permit the distribution, sale, and consumption in the United States of remaining inventories of CFC epinephrine inhalers manufactured pursuant to the exception for medical devices under the Clean Air Act;
(2) not take any enforcement action or otherwise seek to restrict the distribution, sale, or consumption of such inhalers on the basis of any federal law implementing the Montreal Protocol on Substances that Deplete the Ozone Layer; and
(3) issue, in response to a request of any distributor or seller of such inhalers, a No Action Assurance Letter stating that the EPA will not initiate an enforcement action relating to the distribution or sale of any such inhaler occurring prior to August 1, 2013.
Defines "CFC epinephrine inhaler" to mean any epinephrine inhaler containing chlorofluorocarbons that was manufactured and classified as over-the-counter before January 1, 2012.
Terminates this Act on August 1, 2013.

House Republican Conference Summary

The summary below was written by the House Republican Conference, which is the caucus of Republicans in the House of Representatives.


This summary can be found at http://www.gop.gov/bill/112/2/hr6190.

Background

According to House Report 112-673, epinephrine inhalers containing chlorofluorocarbons (CFCs), most commonly marketed as Primatene Mist, have been sold in the U.S. without physician's prescription as an over-the-counter (OTC) medicine to provide relief of asthma symptoms for over 40 years. As of December 31, 2011, the manufacture and sale of these inhalers has been banned for the purpose of reducing emissions of ozone depleting substances into the air pursuant to the “Montreal Protocol on Substances that Deplete the Ozone Layer” and Title VI of the Clean Air Act. The shift to CFC-free inhalers is part of a larger transition that has affected many consumer and industrial products over the last several decades. According to a fact sheet on H.R. 6190 provided by the House Committee on Energy and Commerce, to date, no over-the-counter replacement is available. An estimated 1.7 to 2.3 million asthma sufferers in the United States relied on this medication before the ban went into effect.

There is currently a remaining inventory of approximately 1.2 million OTC epinephrine inhalers. According to the FDA, epinephrine users can use the product after December 31, 2011 because the product phase-out only applies to the manufacture and sale of the product after December 31, 2011, as long as the product has not expired. This legislation would direct the EPA to allow for the distribution and sale of the remaining inventories of the inhaler without threat of EPA enforcement actions.

House Energy and Commerce Myth vs. Fact on H.R. 6190 is available here.

EPA fact sheet on the transition to Ozone-Safe Propellants is available here

Summary

H.R. 6190 would direct the EPA to allow the distribution of remaining inventories of the asthma inhaler known as Primatene Mist. Under current EPA regulations, epinephrine’s inhalers containing chlorofluorocarbons (CFCs) have been banned since December 31, 2011. The bill would direct the EPA to refrain from taking any enforcement action against any distributor or seller on the basis of any federal law implementing the Montreal Protocol. The bill would also direct the EPA to issue a “No Action Assurance Letter” to any requesting distributor or seller stating the agency will not initiate such an enforcement action. H.R. 6190 would sunset on August 1, 2013.

The bill would not amend the Clean Air Act or change the environmental protections in the Montreal Protocol. Additionally, it would not limit the FDA’s authority to ensure the safety and effectiveness of the remaining inventory of inhalers. It would not authorize the manufacturing of new CFC inhalers. 

Cost

According to the Congressional Budget Office (CBO), “implementing this legislation would have no significant impact on the federal budget because of the limited amount of EPA resources dedicated to these activities. Pay-as-you go procedures do not apply to H.R 6190 because the bill would not affect direct spending or revenues."

House Democratic Caucus Summary

The House Democratic Caucus does not provide summaries of bills.

So, yes, we display the House Republican Conference’s summaries when available even if we do not have a Democratic summary available. That’s because we feel it is better to give you as much information as possible, even if we cannot provide every viewpoint.

We’ll be looking for a source of summaries from the other side in the meanwhile.

The bill contains the following citations to other parts of U.S. law:

United States Code

The United States Code is the compilation of permanent laws enacted by Congress. Temporary and other non-permanent laws do not appear in the United States Code. (About half of the United States Code is the law itself, called positive law. The other half is merely a compilation of the laws but has no legal significance.)