logo
How to Know Your Medspa Uses Real Botox®: 5 Essential Tips for Consumers

How to Know Your Medspa Uses Real Botox®: 5 Essential Tips for Consumers

PR.com)-- When it comes to cosmetic treatments, Botox® is the gold standard for reducing fine lines and wrinkles. However, with the rise in popularity of injectable treatments, the market has become flooded with counterfeit or diluted products being offered by less-than-reputable providers. Ensuring that you receive genuine Botox® from an experienced, qualified injector is critical—not only for the effectiveness of the treatment but also for your safety.
Dr. Elizabeth Littlefield, Medical Director of dermani MEDSPA®, a top 25 U.S. provider of Botox®, offers these essential tips to help you ensure that your medspa is using genuine Botox® and why it's crucial to do your homework:
1. Beware of Providers Who Call It 'Tox' or Other Generic Terms
One of the first red flags to watch out for is when a provider uses vague or generic terms like 'tox,' 'botulinum,' or other euphemisms instead of calling it Botox®. Botox® is a trademarked product manufactured exclusively by Allergan Aesthetics, and reputable medspas will use the correct name to identify the product.
Providers who shy away from using the trademarked term may be attempting to sell you an off-brand or counterfeit version of Botox®, which can pose serious risks to your health. Always make sure the treatment being offered is the real, FDA-approved Botox® from Allergan.
2. Do an Alle® Provider Search
One of the easiest ways to verify whether a medspa is offering genuine Botox® is by searching for the provider on the Alle® website. Alle® is Allergan's loyalty rewards program for Botox® and other Allergan products, and it only works with providers who are authorized to purchase and administer authentic Botox®.
If your medspa is listed on the Alle® site, it's a good sign that they are sourcing their Botox® directly from Allergan. If they are not listed, it's worth asking questions about where their product comes from—or reconsidering your choice of provider altogether.
3. Look for the Allergan Seal on Their Website
Reputable medspas that use authentic Botox® will often display the Allergan seal of approval on their website. This seal indicates that the provider is recognized by Allergan as an authorized distributor of their products.
When browsing a medspa's website, take a moment to check for this seal. It's a quick and easy way to validate their credibility and confirm that they are using the real deal.
4. Insist on Seeing the Botox® Vial and Lot Number
Before receiving your treatment, ask your provider to open the Botox® vial in front of you and show you the lot number on the packaging. Genuine Botox® comes in distinct vials with clear labeling, including the Allergan name and a specific lot number.
This transparency allows you to confirm that the product being used is authentic and fresh. If a provider is hesitant or refuses to show you the vial and lot number, this should be a major red flag.
5. Ask About Their Status with Allergan
Allergan recognizes its top-performing providers with specific designations based on the volume of Botox® they administer. Providers with a high status with Allergan have extensive experience and a proven track record of delivering authentic treatments.
Dr. Elizabeth Littlefield of dermani MEDSPA® emphasizes the importance of asking about a medspa's Allergan status:
'As a top 25 medical spa in the United States for Allergan, the only true maker of Botox®, we highly recommend that clients educate themselves by asking the right questions whenever they are considering who will be injecting Botox® into their body.'
By choosing a medspa with a strong relationship with Allergan, you can feel confident that you're receiving genuine Botox® from a provider who prioritizes safety and excellence.
Why It's Critical to Choose Real Botox®
Choosing a medspa that uses authentic Botox® is about more than just ensuring the best cosmetic results. Counterfeit or off-brand botulinum toxins can lead to serious health risks, including infections, allergic reactions, and unpredictable outcomes. Genuine Botox® from Allergan has undergone rigorous testing and is FDA-approved, making it a safe and effective option when administered by a qualified provider.
Final Thoughts
When it comes to Botox®, knowing your medspa uses the real product is essential for both safety and results. By following these five tips—avoiding vague terms like 'tox,' doing an Alle® search, checking for the Allergan seal, verifying the vial and lot number, and asking about Allergan status—you can confidently choose a provider who will deliver the quality and care you deserve.
dermani MEDSPA®
Sheanya Samuels
470-835-0183
Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Wel-Bloom Biotech Launches Wel-ROS6. Black Crystal Roselle Sparks a Surge in High-Concentration Anthocyanins
Wel-Bloom Biotech Launches Wel-ROS6. Black Crystal Roselle Sparks a Surge in High-Concentration Anthocyanins

Associated Press

time2 hours ago

  • Associated Press

Wel-Bloom Biotech Launches Wel-ROS6. Black Crystal Roselle Sparks a Surge in High-Concentration Anthocyanins

TAIPEI, TAIWAN - Media OutReach Newswire - 22 July 2025 - Taiwan's leading jelly supplement manufacturer, Wel-Bloom Biotech, recently co-hosted an anthocyanin-focused seminar with LEARN EATiNG, one of the most renowned nutritionist teams in Taiwan. The event highlighted trending international ingredients alongside Taiwan's own Black Crystal Roselle. Attracting around 300 nutrition professionals both online and onsite, the seminar reflected strong industry interest and high expectations for the future of anthocyanin innovation. Wel-Bloom Biotech and the LEARN EATiNG nutrition team host a high-profile seminar. (Image/Wel-Bloom) In recent years, the health supplement market has seen rapid growth, accompanied by a shift in consumer priorities. Today's consumers increasingly believe that 'choosing the right ingredients matters more than simply taking more,' a mindset that is driving innovation in ingredient formulation. According to the 2024 Top 30 Dietary Trends Report, there is growing interest in the synergistic effects of ingredient combinations. For instance, pairing anthocyanins with fish oil offers comprehensive support for overall health, while combining them with collagen enhances beauty and skin wellness. The Black Crystal Roselle, grown locally in Taiwan, contains naturally high levels of anthocyanins and has recently drawn growing interest in the health supplement field for its promising nutritional potential. As one of the keynote speakers, Wel-Bloom Biotech introduced Wel-ROS6®—a proprietary botanical ingredient derived from Black Crystal Roselle. Developed using triple-patented technology, it is cultivated through natural farming methods and smallholder contract farming to ensure consistent quality and traceability. Laboratory data shows that Wel-ROS6® contains 17.7 times more total anthocyanins than standard commercial roselle. Additionally, total phenolic acids and flavonoids are elevated by 1.9 times and 1.3 times, respectively—highlighting its rich phytochemical profile and high functional value. (See Note 1) The event also featured the Food Industry Research and Development Institute's newly proposed 'Food Value Equation": Value = (Sensory Perception × Functional Technology × User Experience) × Amplification Multiplier. This formula highlights the importance of balancing sensory appeal, technological innovation, and user experience—emphasizing that all three elements are essential to creating meaningful value in food products. To meet growing consumer demands for convenience and palatability in health supplements, product development is increasingly focused on factors such as absorption efficiency, flavor optimization, and sustainable sourcing. The rise of 'tasty' health products reflects a major trend in preventive wellness—perfectly aligned with today's mindset of 'eating less, supplementing smarter.' Through its one-stop CDMO (Contract Development and Manufacturing Organization) services, Taiwan's local agriculture can now be transformed from raw materials into globally market-ready products that seamlessly integrate into everyday life. Wel-ROS6®, backed by the support of over 300 health professionals, will be featured alongside other cutting-edge botanical ingredients at the 2025 BIO Asia–Taiwan Exhibition and Vitafoods Asia. We warmly invite you to visit our booth and explore partnership opportunities with Wel-Bloom Biotech to co-create the next generation of best-selling health supplements. Note 1: Testing commissioned to the Food Industry Research and Development Institute: Independent testing by the Forecast Research Lab: Hashtag: #Welbloom #Wel-ROS6 #BlackCrystalRoselle The issuer is solely responsible for the content of this announcement.

Makary ally named to key FDA drug post
Makary ally named to key FDA drug post

Politico

time3 hours ago

  • Politico

Makary ally named to key FDA drug post

With help from Robert King Driving the Day CDER'S NEW LEADER — Dr. George Tidmarsh, a Stanford pediatrics adjunct professor and former pharmaceutical executive, is FDA Commissioner Marty Makary's pick to be the nation's top drug regulator. The new Center for Drug Evaluation and Research director has a history with Makary as a contributor to the Journal of the Academy of Public Health, an alternative journal the FDA chief helped launch. Additionally, Tidmarsh spoke at FDA headquarters during Makary's inaugural roundtable discussion on agency-regulated products, praising him for convening the unconventional event so quickly into his tenure. 'You're a person of action, and you care about the public, based on your question and making this a public event,' Tidmarsh said. The former Horizon Pharma founder helped develop the rheumatoid arthritis treatment Duexis — a combination of ibuprofen and the histamine blocker famotidine. He also founded Threshold Pharmaceuticals and was a senior employee at Coulter Pharmaceutical and SEQUUS Pharmaceuticals, according to a Stanford Medicine bio. Already at White Oak: Tidmarsh was on the FDA campus Monday for his first day. 'The number one thing I need to work on is motivating people,' Tidmarsh said in an FDA podcast posted Monday afternoon. 'That's the one thing that is most important coming here.' Tidmarsh also laid out his personal views on the FDA's role in regulating emerging technologies like gene therapies. 'In larger populations, of course, you need to demand the strong, irrefutable data of statistical and clinical significance,' Tidmarsh said. 'But there's going to be times where judgment has to come into play, especially for very small populations.' The Association for Accessible Medicines and the Biosimilars Council quickly praised the pick. 'We look forward to a collaborative partnership with Dr. Tidmarsh and the larger team at CDER to prioritize regulatory efficiency and help ensure the medicines that cost less and make up 90 percent of all prescriptions filled in the U.S. are always available for patients,' AAM CEO John Murphy said in a statement. One thing to keep an eye on is how Tidmarsh fits into an agency that has seen a number of top longtime regulators depart in the past year. 'Tidmarsh's industry background should nevertheless be reassuring to sponsors, though it may be something of a double-edged sword for him as he fits into the broader Trump administration dynamics,' TD Cowen's Rick Weissenstein wrote in a research note. IT'S TUESDAY. WELCOME BACK TO PRESCRIPTION PULSE. Your host has been hit hard by a nasty cold he hears is circulating on Capitol Hill. Send tips to David Lim (dlim@ @davidalim or davidalim.49 on Signal) and Lauren Gardner (lgardner@ @Gardner_LM or gardnerlm.01 on Signal). Eye on the FDA FDA V. SAREPTA — The FDA and Sarepta Therapeutics were at odds over the agency's request that the company halt shipments of its Duchenne muscular dystrophy gene therapy, Elevidys. But late Monday, the company agreed to temporarily pause at the close of business on Tuesday. Late Friday, the company put out a news release that said it 'received an informal request' to 'voluntarily halt shipment' of the medicine. 'Based on our comprehensive scientific interpretation of the data, which shows no new or changed safety signals in the ambulant patient population, we will continue to ship ELEVIDYS to the ambulant population,' Sarepta said in the release. But Sarepta took a different tack Monday. 'As a patient-centric organization, the decision to voluntarily and temporarily pause shipments of ELEVIDYS was a painful one, as individuals with Duchenne are losing muscle daily and in need of disease-modifying options,' Sarepta CEO Doug Ingram said in a news release. 'It is important for the patients we serve that Sarepta maintains a productive and positive working relationship with FDA, and it became obvious that maintaining that productive working relationship required this temporary suspension while we address any questions that FDA may have and complete the ELEVIDYS label supplement process.' Before the announcement by Sarepta, HHS spokesperson Andrew Nixon said the FDA was 'deeply disappointed' in the drugmaker's decision Friday. 'We are deeply troubled that the company insists on dosing additional patients with Elevidys while we investigate this concerning safety signal,' Nixon said in an email. 'FDA will remain flexible but will move swiftly when a product presents an unreasonable and significant risk and will leverage our full regulatory authority to pursue a course of action that protects patients.' LOOMER GOES AFTER PRASAD — Right-wing activist Laura Loomer is taking aim at top FDA vaccine regulator Dr. Vinay Prasad. A Sunday post on Loomer's website points to a litany of remarks Prasad made before he joined the agency earlier this year — arguing he is not aligned with President Donald Trump's agenda. 'Allowing a trojan horse wield such power is a mistake that threatens the very reforms Trump was elected to deliver,' Loomer wrote. 'The time to act is now — Prasad must go before he completely destroys the [Make America Healthy Again] movement and all of the hard work President Trump has put into his regulatory reform agenda.' HHS spokesperson Andrew Nixon declined to comment on the Loomer remarks. Loomer has previously targeted other influential health policy figures she sees as disloyal to Trump. In May, she called out Brian Blase, president of Paragon Health Institute, for his positions on Medicaid. Industry Intel COMING TO A TOWN NEAR YOU — U.K. pharma giant AstraZeneca announced plans to build a new, multibillion-dollar plant in Virginia to manufacture weight-loss drugs, chronic disease medicines and other drug therapies, Robert reports. The announcement on Monday in Washington is part of a larger $50 billion investment from the drugmaker to boost manufacturing and research within the country. The move comes amid threats from President Donald Trump to hit pharmaceutical companies with steep tariffs if they do not take steps to manufacture products in the U.S. 'The U.S. leads innovation in pharmaceuticals, but China is moving very quickly … and we need to continue moving as quickly as we can in the U.S. to keep this leadership,' said CEO Pascal Soriot during the event. The exact plant location remains unclear but once completed would be the 'largest single manufacturing investment in the world,' according to a release from the manufacturer. It would produce GLP-1 weight-loss drugs as well as a combination of small-molecule drugs, the company said. AstraZeneca has also pledged to expand its research and development facility in Gaithersburg, Maryland, as well as new sites to supply clinical trials. Soriot acknowledged that the potential of pharmaceutical tariffs is 'accelerating the movements, whether with us or others.' However, he added that he understood the need for a country like the U.S. to want to see products, medicines serving patients in this country to be manufactured in the country. It's a question of national security.' AROUND THE AGENCIES HEARING THEM OUT — NIH Director Jay Bhattacharya met Monday with 38 staffers who had signed an open letter to him last month, addressing their concerns about grant terminations, staff firings and the politicization of science since President Donald Trump took office, Erin reports. At a rally after the meeting, staffers who attended the roundtable described it as cordial but said Bhattacharya made no promises to reverse agency policy. Bhattacharya welcomed 'open, constructive input' on NIH's future, according to HHS spokesperson Andrew Nixon. 'The ability to question, challenge and share ideas is central to the scientific method,' he added. During the meeting, Bhattacharya said he wouldn't retaliate against NIH staffers for signing the so-called Bethesda Declaration, the name the agency employees used for the letter. The open letter was modeled after the Great Barrington Declaration, which Bhattacharya co-authored in 2020 to protest pandemic lockdowns. Hundreds of NIH staffers from every institute and center signed it, as did Nobel laureates, former NIH institute and program directors and other leaders in the scientific community. Earlier this month, the Environmental Protection Agency placed 139 employees on administrative leave for writing an open letter criticizing EPA Administrator Lee Zeldin for regulatory rollbacks, funding cuts and staff firings at the agency. What's next: Bhattacharya expressed openness about future roundtables, attendees said, but no meetings have been scheduled. Pharma Moves Sonja Fulmer, acting director of the FDA's Digital Health Center of Excellence within the Center for Devices and Radiological Health, is leaving the agency, according to an FDA employee and a former FDA employee granted anonymity to discuss the departure, POLITICO's Ruth Reader reports. Fulmer, who has been at CDRH for more than 10 years, took over for former DHCoE Director Troy Tazbaz after he left in January. HHS did not immediately return a request for comment. Document Drawer The FDA released draft guidance on the International Council for Harmonisation's guidelines for including pregnant and breastfeeding women in clinical trials. FDA Commissioner Marty Makary and agency chief of staff Jim Traficant met with Arnold Ventures to discuss 'items of mutual interest' on July 8, according to a newly posted public calendar disclosure. Makary also met with Sen. James Lankford (R-Okla.) the same day for an introductory meeting. On July 10, Makary met with Rep. Jamie Raskin (D-Md.) for an introductory meeting. WHAT WE'RE READING The New York Times' Sarah Kliff reports on health insurers denying more and more drug claims. The Congressional Budget Office said cuts to the NIH and the FDA would slow drug approval and development, POLITICO's Simon Levien reports.

Sarepta Therapeutics says it will pause shipments of Duchenne gene therapy
Sarepta Therapeutics says it will pause shipments of Duchenne gene therapy

Boston Globe

time3 hours ago

  • Boston Globe

Sarepta Therapeutics says it will pause shipments of Duchenne gene therapy

'This proactive step will allow Sarepta the necessary time to respond to any requests for information and allow Sarepta and FDA to complete the Elevidys safety labeling supplement process,' said Sarepta CEO Doug Ingram, in a statement. The decision wasn't entirely in Sarepta's control. On Monday, Children's Hospital Los Angeles (CHLA) said it was pausing use of Elevidys while the drug is in regulatory limbo. Get Starting Point A guide through the most important stories of the morning, delivered Monday through Friday. Enter Email Sign Up 'Patient safety is paramount at CHLA and the hospital has communicated its decision with affected patient families while it awaits any further determination by the FDA,' the hospital told STAT. Advertisement Other hospitals that specialize in the treatment of Duchenne patients are reportedly considering similar treatment pauses. Sarepta may have also realized that fighting with the FDA was high-risk. 'It is important for the patients we serve that Sarepta maintains a productive and positive working relationship with FDA, and it became obvious that maintaining that productive working relationship required this temporary suspension,' said Ingram, in the statement. Sarepta did not indicate how long the Elevidys suspension might last. Ritu Baral, a biotech analyst at Cowen, estimated 3 to 6 months. During that time the company would test a proposed immune-suppressing protocol designed to mitigate the serious liver toxicity caused by the gene therapy, and share those data with the FDA. Advertisement In a statement, Parent Project Muscular Dystrophy, a patient advocacy organization, said the FDA demand to halt Elevidys shipments and Sarepta's agreement to do so has 'intensified concerns and uncertainty' for Duchenne patients and their families. 'We deeply value the importance of data-driven decision-making and responsible regulatory oversight. We urge both Sarepta and the FDA to communicate with urgency, clarity, and transparency about the path forward,' the group said. On Friday, the FDA asked Sarepta to pause all shipments of Elevidys following media reports of the death of a 51-year-old man who received a different but related gene therapy for a different form of muscular dystrophy. That death followed the deaths in March and June of two teenagers who received Elevidys. Sarepta had already paused shipments for patients who rely on wheelchairs — boys with Duchenne typically lose the ability to walk around age 12. But the company initially said it would not comply with the FDA's request to also halt shipments for ambulatory patients. To agree would mean a de facto withdrawal of the therapy from the market. But on Monday, the company reversed course. Elevidys has appeared safer and more effective in ambulant Duchenne patients, who are generally younger, but significant side effects can still occur. Scheduled infusions across the country will now be canceled.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into a world of global content with local flavor? Download Daily8 app today from your preferred app store and start exploring.
app-storeplay-store