
What Dermatologists Have to Say About Using Beef Tallow for Your Skin
On TikTok, there's a place for everything, especially skincare. The latest trend is all-natural beef tallow, or rendered beef fat, to hydrate, prevent blemishes and more. This is part of a movement to return to basic care and chemical-free products.
While you may be used to beef tallow as a kitchen staple (it's most commonly used as an oil for frying, giving your dishes a light beef flavor), this simple product can be used for many other things as well. It's been tested as a household product over the years, and social media has now brought it to the masses.
However, it hasn't been studied closely as a skincare ingredient, so as with any new product that you want to try, do so with caution and consult your dermatologist before jumping on the bandwagon.
Below, learn more about all the buzz around beef tallow, including the potential benefits and drawbacks.
Read more: Easy Ways to Improve Your Skin's Glow
What is beef tallow?
Beef tallow is the product of clarifying fatty tissue from around the organs of a cow. At room temperature, it's solid and often used in cooking. It can also be used in things like soap, candles and other skincare products because of its creamy texture and oiliness.
According to the Mayo Clinic, beef tallow is primarily made up of saturated fats due to its solid nature. It also has saturated and polyunsaturated fats. Beyond fats, beef tallow contains fat-soluble vitamins and essential fatty acids, which has made it an attractive cooking ingredient.
Beef tallow rave on TikTok
Beef tallow has recently surged in popularity, thanks in large part to social media. Content creators on TikTok have been touting its claims, saying the natural product is giving them incredible skin. One user posted a video in January saying beef tallow "healed my skin barrier."
The belief is that beef tallow can hydrate skin and help protect the skin barrier. Some even believe it can act as an anti-inflammatory and help relieve blemishes. This can vary greatly, though, depending on each person's skin -- as with any skincare product and regimen. The benefits of your beef tallow can also vary based on your cows. The Mayo Clinic states the grass-fed cows will have a more robust vitamin profile in their tallow than those on a conventional diet.
Tallow has a similar texture and appearance to coconut oil, and as a beauty product, it's almost balm-like. Some of these beauty fans are even making their own beef tallow products at home, rendering the tallow themselves, as it just requires boiling down the fat over the stove. You can also get the fat from your local butcher. If you don't want to DIY, you can buy premade beef tallow products online for under $20.
What experts have to say about beef tallow
Dr. Teresa Song, a board-certified dermatologist at Marmur Medical, sees some benefits in using beef tallow as a skincare product but cautions most people against trying it.
"It is probably better tolerated for dry skin and should be avoided in those with sensitive skin, combination, acne and oily skin types due to potential worsening of breakouts," she tells CNET.
However, for those who can tolerate it, Dr. Song notes that it can be a worthwhile skincare product if chosen carefully and used properly. Though it hasn't yet been widely studied, it is believed to mimic human vitamin profiles -- A, D, E, K and B12 -- which may offer benefits for certain skin types. She also highlights its role in promoting hydration for very dry skin, making it worth considering for those with the right skin type.
AleksandarNakic/Getty Images
As some on TikTok have experienced, the thick texture of beef tallow can be problematic. That's why Dr. Song doesn't recommend it for sensitive skin, as it can lead to breakouts rather than help with acne. She also stressed the fact that it is an animal product and that some people may have an allergic reaction.
Beyond the risk of an allergic reaction, the animal-based nature of tallow is another concern, Dr. Song notes, as it has a higher potential to spoil. In contrast, plant-based moisturizers like shea or cocoa butter are more stable.
"Modern ingredients are also more studied and processed as compared to beef tallow," she adds, continuing, "Modern skincare ingredients like hyaluronic acid, squalene and ceramides tend to offer targeted hydration without greasiness as compared to beef tallow. Sources of the beef tallow need to be more standardized and use should be individualized."
Sustainability and ethical considerations
Though vegans and vegetarians would disagree with using beef tallow, those who believe in not letting any part of an animal go to waste would support using pieces that might normally be thrown out. Fat isn't often valued, and finding an additional use for the beef tallow (beyond just cooking with it) creates less waste.
However, it is a meat product, and the most ethical way to source it is to find cows that are farmed responsibly and taken care of in a sustainable environment. These cows are usually grass-fed and pasture-raised. Plus, when you get tallow from cows raised this way, they're often healthier, which means a higher quality of tallow.
For vegans and vegetarians, the alternative is to find a plant-based product, which is what many of the other beauty products on the market already are.
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Medscape
38 minutes ago
- Medscape
Population-Level Weight Loss Seen With Primary Care Protocol
CHICAGO — Encouraging patients to talk with their primary care physicians about weight management led to increased visits for obesity, population-wide weight loss, and increased revenue, researchers at the University of Colorado Anschutz School of Medicine (CU Anschutz) reported here at the American Diabetes Association (ADA) 85th Scientific Sessions. The researchers presented data from a 4-year study of the PATHWEIGH protocol, which was implemented at 56 primary care clinics across Colorado. Ultimately, 274,182 patients were part of the study, which has not yet been published. Although weight loss was low in the intervention group — 0.1 kg at 18 months — the intervention eliminated the typical expected weight gain population-wide. And indeed, that weight gain was about 0.1 kg in those who did not receive the intervention. "Our data is the first to scale an intervention to more than a quarter of a million people and prevent population weight gain," said Leigh Perreault, MD, associate professor of medicine in the division of endocrinology, metabolism and diabetes at CU Anschutz, who presented the data. Using a stepped-wedge cluster randomized trial design, researchers randomized clinics to offer usual care or the intervention. Each clinic eventually moved to using the intervention. Patients who received usual care would have visits during which weight could be discussed but clinicians did not have access to PATHWEIGH tools. Those who received the intervention had weight-specific visits and their doctors had access to the protocol. The Colorado group created PATHWEIGH to help primary care physicians fill the gap in obesity care in the face of growing numbers of overweight and obese Americans. Patients in the usual care or intervention group were alerted to the opportunity to have a weight-prioritized visit with their primary care physician. In the intervention group, patients were asked to complete a weight-management questionnaire before the visit, which the physician could then use as a prompt to talk with the patient during the visit. Researchers also provided clinicians with specialized support tools, education, and most importantly, a weight-specific template embedded in the electronic medical record. The template allowed for diagnosis, documentation of a weight-related discussion (for reimbursement), and orders for referrals, tests, and procedures, which streamlined workflow and made it easier to help patients, said Perreault. Physicians were asked to follow up with patients at least every 4 to 6 weeks. Use of the tools was optional, however. This meant that patients in the intervention group could get usual care with or without PATHWEIGH. At baseline, the mean age of patients was 54 years. About 53% were female, and 78% were non-Hispanic White, 11% Latino, 4% Black, and 2% Asian. Two thirds had commercial insurance and about a third were Medicare enrollees. Mean BMI was 31 kg/m2. At the end of the 4-year study, researchers found only about 25% of patients with a BMI of 25 kg/m2 or more received any discernible care for their weight, said Perreault. Discernible care might include adequate counseling about diet, exercise, and behavioral modification, referral to a dietitian or bariatric surgeon, or prescription of an anti-obesity medication. More people in the intervention group received such care. Those most likely to receive care had a BMI of at least 25 kg/m2, tended to be closer to age 50, were commercially insured, and were Latino or Black. However, said Perreault, an A1c in the prediabetes range, an estimated glomerular filtration rate in the stage 2 chronic kidney disease range, or the presence of a weight-related disease or complication did not prompt clinicians to offer help. Patients who did receive weight-related care during the intervention lost 2.37 kg more than those in the intervention group who received no care. Getting any sort of help with weight management made a difference, even outside the intervention. Those who received usual care offered weight management assistance lost 1.73 kg more than patients in the usual care group who received no care. Perreault said that providers spent no extra time on weight-prioritized visits and that using weight-related International Classification of Diseases 10 codes added more than $15 million to the health system's revenues over the 4-year study. PATHWEIGH outreach also resulted in "more than twice as many" visits for weight management, she said. 'Monumental' But Not 'Hugely Successful' "This is monumental work," said Ildiko Lingvay, MD, MPH, MSCS, a professor of internal medicine at University of Texas Southwestern Medical Center, Dallas, who chaired the session during which the study results were presented. Changing population weight by a pound is "like moving mountains," she said. However, added Lingvay, "It's not that I think this intervention was hugely successful." She's excited to see how the intervention works as it is adopted by others. Robert Kushner, MD, MS, a professor of medicine at Northwestern University Feinberg School of Medicine, Chicago, Illinois, offered the Colorado group "a big congratulations." "This is a really tough nut to crack," said Kushner, who was asked for comment. "There are significant barriers and challenges to treating obesity in primary care," he said. Many approaches basically remove the primary care physician from the equation by diverting patients to online platforms, coaching, or self-help, or weight-loss programs. "Embedding" the primary care physician is "the road less taken, to be honest," said Kushner, which PATHWEIGH successfully does. And it is an "innovative program for a healthcare system, population-level approach to the management of obesity." Looking ahead, the researchers should determine how to increase both clinician and patient engagement, said Kushner. It would also be useful to examine what triggers referrals to other services and to assess clinical outcomes and mediators of weight change, he said. Lastly, researchers should "determine the use and effectiveness of obesity medications. That's extremely important in the day we live," said Kushner. The study was funded by the National Institute of Diabetes and Digestive and Kidney Diseases. Perreault has disclosed receiving personal fees for speaking and/or consulting from Novo Nordisk, Eli Lilly, Boehringer Ingelheim, Ascendis, Medscape, WebMD, and UpToDate. Lingvay has reported consulting for AbbVie, Altimmune, Amgen, Alveus, Antag Therapeutics, AstraZeneca, Bayer, Betagenon, Bioio, Biomea, Boehringer Ingelheim, Carmot, Cytoki Pharma, Eli Lilly, Intercept, Janssen/J&J, Juvena, Keros Ther, Novo Nordisk, PharmaVentures, Pfizer, Regeneron, Roche, Sanofi, Shionogi, Source Bio, Structure Therapeutics, Target RWE, Terns Pharmaceuticals, The Comm Group, WebMD, and Zealand Pharma. Kushner has reported no conflicts related to PATHWEIGH but disclosed being a board member for Altimmune, Currax, Novo Nordisk, Structure Therapeutics, and Weight Watchers International, and a consultant for Eli Lilly and Regeneron.
Yahoo
an hour ago
- Yahoo
BioAge Labs to Present Preclinical Data on APJ Agonism for Diabetic Obesity and Heart Failure at the American Diabetes Association (ADA) 85th Scientific Sessions
Treatment with apelin receptor agonist enhanced glycemic control and demonstrated cardioprotective effects, with additive benefits observed in combination with incretin therapy Data support development of next-generation APJ agonists for obesity and key comorbidities EMERYVILLE, Calif., June 21, 2025 (GLOBE NEWSWIRE) -- BioAge Labs, Inc. (Nasdaq: BIOA) ('BioAge', 'the Company'), a clinical-stage biotechnology company developing therapeutic product candidates for metabolic diseases by targeting the biology of human aging, today announced that it will present new preclinical data supporting apelin receptor (APJ) agonism for the treatment of diabetic obesity and heart failure with preserved ejection fraction (HFpEF). The data will be presented at the American Diabetes Association's 85th Scientific Sessions, held June 20–23, 2025, in Chicago, Illinois. 'Our preclinical data demonstrated that APJ activation can confer multiple benefits in models of diabetic obesity and heart failure, and enhance the effects of incretin therapy,' said Kristen Fortney, PhD, CEO and co‑founder of BioAge. 'We are advancing next‑generation APJ agonists to translate this promising biology into new therapies for obesity and its major comorbidities.' APJ is the receptor for apelin, an exercise-induced signaling molecule known as an exerkine. Apelin has been shown in preclinical studies to have the potential to recapitulate many of the downstream benefits of exercise. BioAge's discovery platform identified apelin signaling as a therapeutic target based on analysis of human aging cohorts, which revealed that higher levels of circulating apelin are predictive of improved physical function and increased longevity. BioAge has shown that in preclinical obesity models, APJ agonism can approximately double the weight loss induced by GLP-1 receptor agonists while restoring body composition and muscle function, suggesting that APJ agonists could serve as pharmacological exercise mimetics to enhance incretin therapy. BioAge is advancing multiple APJ agonist approaches, including both oral small-molecule and long-acting injectable formulations, with an IND filing targeted for 2026 [link]. In their two presentations, BioAge CMO and EVP Research Paul Rubin, MD, and scientist Shijun Yan, PhD, MBA, will present data that demonstrated that in preclinical models of diabetic obesity and HFpEF, APJ agonist treatment had potential as monotherapy that could be enhanced in combination with incretin therapies. —Dr. Rubin's oral presentation will show that in mouse models of diabetic obesity, APJ agonist monotherapy reduced HbA1c to levels comparable to lean controls and improved glucose tolerance by 25%. When combined with an incretin, APJ agonism further improved glycemic control compared to the incretin alone. Currently, fewer than half of patients with type 2 diabetes achieve optimal glycemic control on current incretin therapies. — Dr. Yan's poster will show that in a mouse model of obesity-associated heart failure, APJ agonist monotherapy reduced cardiac hypertrophy and suppressed markers of cardiac injury. Combination of APJ agonism with an incretin provided enhanced cardioprotective benefits and greater weight loss compared to either treatment alone. Over half of heart failure patients have preserved ejection fraction, and approximately two-thirds of these patients have obesity. Current therapeutic options for obesity-associated HFpEF remain limited. Oral presentation: Saturday Jun 21, 2025 5:00 PM - 5:15 PM CDTTitle: An Oral Apelin Receptor Agonist Enhances Glycemic Control in Preclinical Models of Diabetic Obesity Both as Monotherapy and in Combination with TirzepatideSession: Early Phase, Post Hoc, and Subgroup Analyses from Clinical Trials Testing Incretin-Based Therapies—Take 1; W181 A-CPresenter: Paul Rubin, MD, Chief Medical Officer and EVP-Research Poster presentation: Sunday Jun 22, 2025 12:30 PM - 1:30 PM CDTTitle: The Apelin Receptor Agonist Azelaprag Shows Cardioprotective Effects as Monotherapy and Enhanced Benefits with Semaglutide in a Diet-Induced Obesity Model of Heart Failure with Preserved Ejection FractionSession: Poster Hall F1, Board No. 866Presenter: Shijun Yan, PhD, MBA, Senior Scientist, In Vivo Biology The visual materials for the presentations will be made available on the BioAge investor website concurrent with the beginning of their respective sessions. About BioAge Labs, Inc. BioAge is a clinical-stage biopharmaceutical company developing therapeutic product candidates for metabolic diseases by targeting the biology of human aging. The Company's lead product candidate, BGE-102, is a potent, orally available, brain-penetrant small-molecule NLRP3 inhibitor being developed for obesity. BGE-102 has demonstrated significant weight loss in preclinical models both as monotherapy and in combination with GLP-1 receptor agonists. IND submission and initiation of a Phase 1 SAD/MAD trial are planned for mid-2025, with initial SAD data anticipated by end of year. The Company is also developing long-acting injectable and oral small molecule APJ agonists for obesity. BioAge's additional preclinical programs, which leverage insights from the Company's proprietary discovery platform built on human longevity data, address key pathways involved in metabolic aging. Forward-looking statements This press release contains 'forward-looking statements' within the meaning of, and made pursuant to the safe harbor provisions of, the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including, but not limited to, statements regarding our plans to develop and commercialize our product candidates, including BGE-102 and our APJ program, the timing and results of our planned clinical trials, risks associated with clinical trials, including our ability to adequately manage clinical activities, the timing of our IND filing for BGE-102 or our APJ program, our ability to obtain and maintain regulatory approvals, the clinical utility of our product candidates or their ultimate ability to treat human disease, the expected timeline for completing proteomic analysis, anticipated analytical results and the potential for identifying novel therapeutic targets, and general economic, industry and market conditions. These forward-looking statements may be accompanied by such words as 'aim,' 'anticipate,' 'believe,' 'could,' 'estimate,' 'expect,' 'forecast,' 'goal,' 'intend,' 'may,' 'might,' 'plan,' 'potential,' 'possible,' 'will,' 'would,' and other words and terms of similar meaning. These statements involve risks and uncertainties that could cause actual results to differ materially from those reflected in such statements, including: our ability to develop, obtain regulatory approval for and commercialize our product candidates; the timing and results of preclinical studies and clinical trials; the risk that positive results in a preclinical study or clinical trial may not be replicated in subsequent trials or success in early stage clinical trials may not be predictive of results in later stage clinical trials; risks associated with clinical trials, including our ability to adequately manage clinical activities, unexpected concerns that may arise from additional data or analysis obtained during clinical trials, regulatory authorities may require additional information or further studies, or may fail to approve or may delay approval of our drug candidates; the occurrence of adverse safety events; failure to protect and enforce our intellectual property, and other proprietary rights; failure to successfully execute or realize the anticipated benefits of our strategic and growth initiatives; risks relating to technology failures or breaches; our dependence on collaborators and other third parties for the development of product candidates and other aspects of our business, which are outside of our full control; risks associated with current and potential delays, work stoppages, or supply chain disruptions, including due to the imposition of tariffs and other trade barriers; risks associated with current and potential future healthcare reforms; risks relating to attracting and retaining key personnel; changes in or failure to comply with legal and regulatory requirements, including shifting priorities within the U.S. Food and Drug Administration; risks relating to access to capital and credit markets; and the other risks and uncertainties that are detailed under the heading 'Risk Factors' included in BioAge's Quarterly Report on Form 10-Q filed with the U.S. Securities and Exchange Commission (SEC) on May 6, 2025, and BioAge's other filings with the SEC filed from time to time. BioAge undertakes no obligation to publicly update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or Chris Patil, media@ IR: Dov Goldstein, ir@ Partnering: partnering@ Web:
Yahoo
2 hours ago
- Yahoo
British tourist catches Legionnaires' disease in Greece
A British tourist is in hospital after catching a serious lung disease while on an all-inclusive holiday in Greece. Donna Jobling, from west Hull, contracted Legionnaires' disease on the island of Crete and is in intensive care. The 57-year-old, who husband Sid, 69, remains at her bedside, was travelling with easyJet Holidays, which said it had moved other customers out of the hotel where she was staying. "We're so sorry to hear that Ms Jobling is unwell, and we're continuing to support her and her family in every way we can," a spokesperson said. Legionella bug delays £41m health centre opening Ms Jobling has been in an intensive care unit at Venizeleio Hospital in Heraklion since 11 June, her niece Klaire Keita told the BBC. On 5 June she developed a chest infection which triggered acute respiratory failure and pneumonia, her niece added. "We just don't know what's going to happen. We're just trying to do the best we can for her," she said. Fighting back tears, Ms Keita added: "She is just the best person you could ever hope to meet." She said her aunt was "stable but under constant watch". Ms Jobling and her husband were holidaying with another couple, Paula and Nicholas Mason, also from Hull. They returned home on 12 June - the day the couples were meant to fly back together. Ms Mason, 52, said: "I felt awful having to leave my best friend there. "Donna has a heart of gold. She would do anything for anyone. We are all still in shock." Ms Mason said photographs of her friend taken at the start of the break showed her "looking really healthy". "Nicolas and Sid had booked the trip as a surprise for us women. Donna was really looking forward to it." Following Ms Jobling's diagnosis, the Greek health ministry issued a statement to hoteliers in Crete to "raise awareness among all those involved in monitoring the quality of water for human consumption especially with regard to Legionella". The source of the disease has not yet been identified but easyJet Holidays has moved other customers out of the hotel they were staying in, as a precaution. "We've also been in touch with customers who recently returned home from this hotel, to inform them of necessary guidance," a spokesperson said. "Our customers' safety and wellbeing is our top priority, and we'll continue to do all we can to support them." It is understood the hotel affected is currently working with local health authorities on the island. An emergency alert has been issued on the island by the European Centre for Disease Prevention and Control following the diagnosis. Legionnaires' disease is a lung infection most commonly contracted through the inhalation of water droplets containing Legionella bacteria. It is usually caught in places such as hotels, hospitals and office buildings from contaminated air conditioning systems, but can also be contracted from spa pools and hot tubs. Symptoms include shortness of breath, a high temperature and chest pain or discomfort, particularly when breathing or coughing. The disease can induce pneumonia and other respiratory illnesses, which can be life-threatening. Smokers, people over the age of 50 and those who are immunocompromised or have chronic lung conditions are at higher risk of developing the disease. A Foreign, Commonwealth & Development Office spokesperson said: "We are supporting the family of a British woman in hospital in Greece and are in contact with the local authorities." Legionella bug closed mental health ward - report