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Press Releases

A win for human rights: DC mayor’s signature is a major step in banning child marriage

January 24, 2025
January 24, 2025: Washington, DC – The National Consumers League (NCL) applauds Washington, DC Mayor Muriel Bowser for signing the Child Marriage Prohibition Amendment Act of 2024 into law. This important legislation prohibits child marriages in the District of Columbia, ensuring the protection of minors from this harmful practice. The bill will now undergo 30 days of congressional review. If approved by Congress, the District of Columbia will join the 13 U.S. states and two U.S. territories that have already banned child marriage.
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https://nclnet.org/wp-content/uploads/2024/10/shutterstock_716651863-scaled.jpg 1707 2560 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-01-24 22:10:162025-05-07 23:56:35A win for human rights: DC mayor’s signature is a major step in banning child marriage

NCL supports click-to-cancel legislation in Maryland Senate

January 21, 2025
January 21, 2025: Washington, DC – Today, NCL submitted testimony in support of SB49 before a Thursday hearing in the Maryland Senate Finance Committee.
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NCL applauds DOL’s efforts to hold corporations accountable when it comes to child labor violations

January 21, 2025
January 21, 2025: Washington, DC – Today, the National Consumers League (NCL) applauds the U.S. Department of Labor (DOL) for their recent efforts to combat unlawful child labor practices, following several significant enforcement actions in the past week. These recent actions demonstrate the Department's commitment to holding corporations accountable for violating child labor laws and protecting vulnerable young workers from exploitation.
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https://nclnet.org/wp-content/uploads/2025/01/factory-work.png 788 940 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-01-21 20:51:072025-05-07 23:56:56NCL applauds DOL’s efforts to hold corporations accountable when it comes to child labor violations

Daniel M. Greene joins NCL as Senior Director of Consumer Protection and Product Safety Policy

January 21, 2025
January 21, 2025: Washington, DC – The National Consumers League (NCL), America’s pioneering consumer advocacy organization, is pleased to announce the appointment of Daniel M. Greene as the new Senior Director of Consumer Protection and Product Safety Policy.
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https://nclnet.org/wp-content/uploads/2025/01/thumbnail_FullSizeRender.jpg 2472 1920 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-01-21 14:32:222025-02-11 19:50:21Daniel M. Greene joins NCL as Senior Director of Consumer Protection and Product Safety Policy

Cecile Richards, a champion of women’s reproductive rights

January 20, 2025
January 20, 2025: Washington, DC – The National Consumers League joins in mourning the untimely death of Cecile Richards, long-time Planned Parenthood president.
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https://nclnet.org/wp-content/uploads/2025/01/Cecile-Richards.jpg 1241 1340 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-01-20 19:41:142025-02-11 19:51:15Cecile Richards, a champion of women’s reproductive rights

NCL celebrates White House’s affirmation of Equal Rights Amendment ratification 

January 17, 2025
January 17, 2025: Washington, DC – Today, the president of the United States affirmed that the Equal Rights Amendment became the 28th amendment to the Constitution when Virginia became the 38th state to ratify the measure in 2020.
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https://nclnet.org/wp-content/uploads/2025/01/women-vote.png 788 940 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-01-17 21:04:502025-05-22 18:18:21NCL celebrates White House’s affirmation of Equal Rights Amendment ratification 

Protecting American Consumers: A Conversation with Sally Greenberg, CEO on Coffee with Ken

January 17, 2025
Janaury 17, 2025: Washington, DC –Sally Greenberg, CEO of the National Consumer League (NCL), was recently the featured guest on Ken Biberaj’s Coffee with Ken. On Protecting American Consumers: A Conversation with Sally Greenberg, they discussed her extensive background in consumer advocacy, the history and monumental victories of NCL, and NCL’s top priorities for 2025 as a new administration is on the horizon.   
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https://nclnet.org/wp-content/uploads/2024/08/coffee-with-ken-for-slider.jpg 723 968 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-01-17 20:39:442025-05-07 23:57:19Protecting American Consumers: A Conversation with Sally Greenberg, CEO on Coffee with Ken

NCL urges timely action to require standardized alcohol content, nutrition and allergen labeling on beer, wine, and distilled spirits products

January 17, 2025
January 17, 2025: Washington, DC – Having pressed the Treasury Department’s Alcohol and Tobacco Tax and Trade Bureau (TTB) for over two decades to require alcohol labeling on beer, wine, and distilled spirits products, the National Consumers League today called for an expedited process to finalize and implement a new TTB rulemaking that will give consumers the same important facts about the content of an alcoholic beverage that is now is readily available on all other beverages, food products, and dietary supplements.
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https://nclnet.org/wp-content/uploads/2025/01/GhgzTGEWYAA2x2u.jpg 570 680 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-01-17 14:48:322025-05-07 23:57:41NCL urges timely action to require standardized alcohol content, nutrition and allergen labeling on beer, wine, and distilled spirits products

NCL applauds DOT’s historic actions to require realistic airline scheduling 

January 16, 2025
Janaury 16, 2025: Washington, DC – The U.S. Department of Transportation (DOT) announced a lawsuit yesterday against Southwest Airlines for chronically delayed flights.
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https://nclnet.org/wp-content/uploads/2025/01/multiple-airplanes.png 788 940 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-01-16 17:44:582025-02-11 19:52:47NCL applauds DOT’s historic actions to require realistic airline scheduling 

NCL releases Top Ten Scams Report of 2024

January 16, 2025
January 16, 2025: Washington, DC – Today, the National Consumers League (NCL) announces our Top Ten Scams report of 2024. The number one scam of 2024 was Prizes, Sweepstakes, and Free Gifting accounting for 38% of reported scams.
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https://nclnet.org/wp-content/uploads/2025/01/fraud-report.png 788 940 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-01-16 17:01:382025-05-07 23:57:49NCL releases Top Ten Scams Report of 2024
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For Media Requests

NCL’s office is open Mon. — Fri., 9am — 5pm, Eastern Time.

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Consumer literacy and teens’ spending habits, education: Lisa Hertzberg

Sally Greenberg

Sally Greenberg joined the National Consumers League as Executive Director on October 1, 2007. The League’s focus is on five key priority areas: fraud, child labor, LifeSmarts, health care, especially the safe use of medications and medication adherence, and food safety and nutrition.

Latest Press Releases

Consumer, Patient Safety, and Public Health Groups Petition the FTC to Stop the Deceptive Online Marketing of Unapproved Weight Loss Drugs

September 23, 2025/in Featured Home - Food & Nutrition, Press release/by Lisa McDonald

September 23, 2025: Washington, DC, – Now that a Presidential memorandum directs the Food and Drug Administration (FDA) to ensure accuracy in direct-to-consumer prescription drug advertising and the September 9 MAHA Report calls on the Federal Trade Commission (FTC) to apply its existing authorities to DTC telehealth companies, the National Consumers League (NCL) and 12 patient safety, pharmacy, women’s health and minority health organizations have submitted a petition asking the FTC to launch an investigation of the deceptive marketing practices of telehealth platforms promoting weight loss drugs.

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https://nclnet.org/wp-content/uploads/2025/09/Web-Images-9.png 788 940 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-09-23 09:00:082025-09-26 18:45:55Consumer, Patient Safety, and Public Health Groups Petition the FTC to Stop the Deceptive Online Marketing of Unapproved Weight Loss Drugs

NHTSA Delays Updates to the Five-Star Safety Rating Program

September 22, 2025/in Featured Home - Consumer Protection, Featured Home - Traffic Safety, Press release/by Lisa McDonald

September 22, 2025: Washington, DC— The National Highway Traffic Safety Administration (NHTSA) postponed the effective date of updates to the New Car Assessment Program (NCAP), which is a Five-Star Safety Rating Program that provides consumers with important information to compare the safety of different vehicles. 

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https://nclnet.org/wp-content/uploads/2025/09/iStock-1044328018.jpg 1414 2121 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-09-22 19:28:502025-10-02 15:18:44NHTSA Delays Updates to the Five-Star Safety Rating Program

NCL Blasts FTC for Undermining Table Saw Safety Standards

September 18, 2025/in Featured Home - Consumer Protection, Press release/by Lisa McDonald

September 18, 2025: Washington, DC – The National Consumers League (NCL) strongly opposes the Federal Trade Commission’s (FTC) recommendation to roll back proposed safety standards for table saws. Each year, an estimated 54,850 Americans suffer blade-contact injuries—including 4,000 amputations—costing victims their livelihoods and society more than $4 billion annually. 

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https://nclnet.org/wp-content/uploads/2025/09/iStock-2195006956.jpg 1414 2121 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-09-18 21:20:042025-09-18 21:20:04NCL Blasts FTC for Undermining Table Saw Safety Standards

National Consumers League Statement on FTC Suit Against Live Nation and Ticketmaster

September 18, 2025/in Featured Home - Consumer Protection, Press release/by Lisa McDonald

September 18, 2025: Washington, DC – The National Consumers League (NCL) today welcomed the announcement that the Federal Trade Commission (FTC) and a bipartisan group of state attorneys general have sued Live Nation and Ticketmaster.  The complaint alleges that Live Nation and its Ticketmaster subsidiary rigged the system with deceptive pricing and shady broker deals, raking in hundreds of millions while sticking fans with billions in bogus fees and inflated prices.  

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https://nclnet.org/wp-content/uploads/2025/09/Web-Images-13.png 788 940 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-09-18 17:20:592025-09-18 18:00:13National Consumers League Statement on FTC Suit Against Live Nation and Ticketmaster

Crackdown on Deceptive Weight Loss Drug Ads Marks Victory for Consumers

September 15, 2025/in Featured Home - Food & Nutrition, Press release, Press releases, health/by Lisa McDonald

September 15, 2025: Washington, DC – Justice delayed was justice denied to millions of Americans who have been exposed to a flood of deceptive advertising about the safety of the same weight loss drugs that the Food and Drug Administration warns are not approved and “could be risky for patients.”

Read more
https://nclnet.org/wp-content/uploads/2025/09/Web-Images-12.png 788 940 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-09-15 15:13:052025-09-26 18:46:43Crackdown on Deceptive Weight Loss Drug Ads Marks Victory for Consumers
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PBPA Commends HHS Funding to Support Maternal and Infant Health

The Preterm Birth Prevention Alliance (PBPA), a coalition of maternal and women’s health advocates dedicated to improving preterm birth outcomes in the United States and addressing its disproportionate impact on women of color, applauds the U.S. Department of Health and Human Services (HHS) for awarding nearly $350 million to states across the country to improve support for safe pregnancies and healthy babies.

“For far too long, U.S. maternal health care has lagged behind that of other developed countries, particularly for women of color,” noted Sally Greenberg, Executive Director of the National Consumers League. “This additional funding will enable local health departments and nonprofits to better address the health care needs of the most vulnerable mothers and their babies.”

The funding, awarded by HHS’ Health Resources and Services Administration (HRSA), will support home visiting services, increase access to doulas, address infant mortality and maternal illness, and improve data reporting on maternal mortality.

“Maternal health care in the U.S. has consistently failed women of color,” Greenberg continued.  “We applaud HHS for this additional funding that will help to improve the maternal health for all mothers and babies, especially women of color and those most at-risk.”

The funding announcement follows the release of a report by the U.S. Commission on Civil Rights which found that Native American women are more than two times more likely to die from pregnancy-related complications than white women in the U.S. This disparity was further exacerbated for Black women in the U.S., who are three to four times more likely to die from pregnancy-related complications than white women.

“In addition to expanding programs to support maternal health, we must increase representation from racially and ethnically diverse groups in research and clinical trials, particularly those studying treatment options to prevent maternal morbidity and mortality,” said Greenberg.  “The need for the additional HHS funding and the report from the Commission on Civil Rights clearly illustrate how critical representative research and real world evidence are to ensuring all mothers and their babies have the same opportunity for the best possible health outcomes.”

Diverse research for a diverse America: The value of equitable, real-world research

August 12, 2021/in Blog, Health, Prevention Blog Post

By Sally Greenberg, NCL Executive Director

While the COVID-19 pandemic has led to hardship for all Americans, it is clear that people of color have been disproportionately burdened. Across the health care continuum, addressing this disparity has become part of the broader conversation about the history of systemic racism and the underlying social determinants of health that negatively affect the mental, physical, and economic health of individuals and entire communities.

The pandemic has underscored persistent health disparities, and there is growing recognition that representation in research and clinical trials can have a profound impact on health outcomes. A lack of representation from racially and ethnically diverse groups in research and clinical trials have typically led to gaps in data, missing the opportunity to assess the full impact of various treatments and drugs across a range of populations. The collection and use of real-world research and data to inform the potential use, risks, and benefits of medical products and treatments can ultimately lead to better health outcomes, particularly for those who have been underrepresented in the past.

Existing efforts to improve inclusion

Efforts to expand diversity and representation in medical research are underway in Congress. Policymakers are encouraging the incorporation of Real World Evidence (RWE) in drug development through the recent Cures 2.0 draft legislation released by Reps. Diana Degette (D-CO-1) and Fred Upton (D-MI-6). While the status quo limits us from effectively reaching underserved populations, the proposed legislation would allow studies that include RWE for some drugs after they have been approved. At the heart of this issue is a growing appreciation that the same therapy can affect different populations in different ways, which is why Cures 2.0 supports collecting data that more accurately reflects the unique experiences and needs of patients across diverse populations.

Recognizing the potential for RWE in maternal health

The lack of representative research in the field of maternal health is undeniable, and its implications are staggering. The dismal state of maternal care in the United States reflects how our health care system has failed women of color, including by not adequately studying treatment options to prevent maternal morbidity and mortality. The need for RWE is clear when you consider the persistent disparities in health outcomes that plague minority communities.

Preterm birth and its disproportionate impact on women of color is a stark illustration of the need to make progress on representative research in maternal health. Preterm birth is the second-largest contributor to infant death in America today. Despite the tremendous physical, emotional, and financial toll that preterm birth continues to take on our country — disproportionately so on women and families of color — not enough therapeutic tools currently exist to prevent it.

Today, “17P,” the only FDA-approved treatment to help reduce the likelihood of spontaneous, recurrent preterm birth in the United States is at-risk of being withdrawn from the market in all its forms, including the branded product and five generic versions. Unfortunately there is conflicting evidence from two different clinical trials, one representative of a diverse U.S. population and another studied in a largely white population in Europe. It’s not a straightforward comparison. If 17P is withdrawn, the women most affected by preterm birth, predominantly women of color, would be left without an FDA-approved treatment option.

The FDA is considering the path forward, including additional data collection through leveraging RWE from past patient use. The success of the first (approval) trial for 17P in the impacted communities signals the importance of RWE. Continued access to 17P is, at its core, a matter of health equity. Black women must not yet again be left vulnerable to a system that historically has overlooked them.

PRETERM BIRTH PREVENTION ALLIANCE APPLAUDS FDA’S GRANTING OF HEARING FOR THE ONLY FDA-APPROVED THERAPIES TO REDUCE RECURRENT PRETERM BIRTH

WASHINGTON, DC, August 26, 2021 –

Preterm Birth Prevention Alliance a coalition of maternal and women’s health advocates dedicated to improving preterm birth outcomes in the United States and addressing its disproportionate impact on women of color, commends the U.S. Food and Drug Administration (FDA) for granting a public hearing to discuss 17P, the only FDA-approved class of branded and generic treatments to reduce preterm birth in indicated patients.

We appreciate the FDA’s willingness to hear directly from individuals facing prematurity and the providers who treat them about their experiences with 17P,” said National Consumer League’s Executive Director Sally Greenberg. “It is an important step towards better understanding variations in efficacy across diverse populations and ensuring all women have an equal chance at the best possible outcomes.”

Last week, the FDA agreed to grant Covis Pharma, the manufacturer of the branded 17P product Makena its request for a public hearing to discuss 17P. Hydroxyprogesterone caproate—or “17P”—has been approved since 2011 and is the only FDA-approved class of treatments to help prevent spontaneous, recurrent preterm birth in the United States. In 2020, the FDA proposed withdrawing 17P in all its forms, including the branded product and its five generic versions, based on conflicting efficacy data from two studies composed of vastly different populations, one predominantly inclusive of women in the U.S. most vulnerable to preterm birth and one not.

“Mothers and birthing people deserve access to the best possible treatments to prevent preterm birth. We cannot achieve birth equity if we study pregnant women as a monolith,” said Blythe Thomas, Initiative Director of 1,000 Days. “It is only by systematically researching the real-world, post-market impact of 17P on individuals from a variety of racial and ethnic backgrounds, while maintaining access for all affected, that we can reduce disparities in maternal and infant health.”

While the hearing date has not yet been set, the Alliance looks forward to sharing the perspectives of affected individuals and their physicians with the agency once the hearing is scheduled and will continue to advocate for at-risk moms and babies of all races and ethnicities.

###

ABOUT THE PRETERM BIRTH PREVENTION ALLIANCE

The Preterm Birth Prevention Alliance (PBPA) is a coalition of maternal and women’s health advocates who share a common concern about the state of preterm birth in the United States and the proposed market withdrawal of 17P, the only FDA-approved class of treatments to help prevent spontaneous, recurrent preterm birth. Formed in 2021 by the National Consumers League, the 15 partners in the PBPA seek to improve preterm birth outcomes in the United States by maintaining access to safe, FDA-approved treatment options and advocating for more diverse medical research that adequately represents the experiences of women and newborns of color. Women of color need a seat at the table. To learn more, visit www.pretermbirthalliance.org

LEADING PATIENT ADVOCATES LAUNCH PRETERM BIRTH PREVENTION ALLIANCE TO PROTECT CRITICAL ACCESS TO THE SOLE FDA-APPROVED CLASS OF THERAPIES TO REDUCE RECURRENT PRETERM BIRTH

WASHINGTON, DC, April 20, 2021 – Today, the National Consumers League (NCL), along with a coalition of patient advocacy organizations dedicated to advancing the health of mothers and infants, announced the launch of the >Preterm Birth Prevention Alliance.

Members of the Alliance are joining forces in an effort to preserve patient access to the only Food & Drug Administration-approved class of treatments for pregnant women who have previously had an unexpected, or spontaneous, preterm birth. Together, Alliance members seek to ensure that the Food & Drug Administration (FDA) hears concerns from the full range of stakeholders about the potential risks and impact of withdrawal for at-risk pregnant women and their providers.

For the fifth year in a row, the U.S. preterm birth rate has increased (to 10.2 percent of births), and preterm birth and its complications were the second largest contributor to infant death across the country. Preterm birth also represents a significant racial health disparity, with Black women in America experiencing premature delivery at a rate 50 percent higher than other racial groups throughout the country.

However, in 2020, the FDA >proposed withdrawing hydroxyprogesterone caproate, commonly called “17P” or “17-OHPC”, the only FDA-approved class of branded and generic treatments to help prevent the risk of preterm birth in women with a history of spontaneous preterm birth. The FDA is currently determining whether to hold a hearing on the status of 17P, based on conflicting efficacy data from two studies composed of vastly different patient populations, one inclusive of women in the U.S. most vulnerable to preterm birth and one not.

“We’re fighting for a more inclusive healthcare system that gives everyone an equal chance to have the best outcomes possible,” said Sally Greenberg, executive director of the National Consumers League. “We don’t believe that removing 17P from the market without gaining a better understanding of who could benefit the most from its use is in the best interests of patients, nor their healthcare providers, particularly as there are no other approved treatment options available.”

To date, 14 organizations have joined NCL to advocate for the health interests of at-risk pregnant women and infants, including: 1,000 Days; 2020 Mom; American Association of Birth Centers; Black Mamas Matter Alliance; Black Women’s Health Imperative; Expecting Health; Healthy Mothers, Healthy Babies Montana; HealthyWomen; Miracle Babies; National Birth Equity Collaborative; National Black Midwives Alliance; National Partnership for Women & Families; Sidelines High-Risk National Support Network; and SisterReach.

“As a trained obstetrician and gynecologist, I know firsthand the impact of preterm birth on Black women and birthing people. I also know that racism – not race – is the driving factor leading the disproportionate impact of preterm birth on Black women and birthing people thereby exacerbating systemic inequities in maternal and infant health. To achieve birth equity, which is the assurance of the conditions of optimal births for all people with a willingness to address racial and social inequities in a sustained effort, we must work to protect and uphold a standard of care for spontaneous, recurrent preterm births and ensure it remains accessible and affordable for all who stand in need,” added Dr. Joia Crear Perry, founder and president of the National Birth Equity Collaborative.

The Preterm Birth Prevention Alliance is calling for the FDA to grant a public hearing to fully consider all of the data, additional research methods, and stakeholder perspectives before deciding whether to withdraw approval of this critical class of therapies. The health of America’s moms and babies warrants the utmost care and consideration.

###

ABOUT THE PRETERM BIRTH PREVENTION ALLIANCE

The Preterm Birth Prevention Alliance is a coalition of maternal and women’s health advocates who share a common concern about the state of preterm birth in the United States and the proposed market withdrawal of 17P, the only FDA-approved class of treatments to help prevent spontaneous, recurrent preterm birth. Formed in 2021 by the National Consumers League, we seek to improve preterm birth outcomes in the United States by maintaining access to safe, FDA-approved treatment options and advocating for more diverse medical research that adequately represents the experiences of women and newborns of color. Women of color need a seat at the table. To learn more, visit www.pretermbirthalliance.org.

Initial support for the Preterm Birth Prevention Alliance is provided by Covis Pharma.

MEDIA CONTACT:

Carol McKay, carolm@nclnet.org

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