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VIVAZEN Launches New Botanical Gummy Line: Feel Great™ Function Meets Great Taste

VIVAZEN Launches New Botanical Gummy Line: Feel Great™ Function Meets Great Taste

Flavor-forward, function-packed, and made to move—wherever life takes you
PHOENIX, AZ, April 8, 2025 (EZ Newswire) -- VIVAZEN, the trusted name in functional plant-based supplements, is proud to announce the launch of its all-new Botanical Gummies—a tasty, convenient, and effective way to help support energy, focus, relaxation, and mood. Backed by the same plant-powered benefits Everyday Heroes™ have come to love, the new gummies deliver the feel-good function of VIVAZEN in a chewable format that fits any lifestyle.
Available now at feelgreatbotanics.com, VIVAZEN Botanical Gummies come in three functional options:
Energy + Focus (Berry Bliss): From busy schedules to big goals, stay sharp and energized with this clarity-boosting blend. Whether you're powering through a workout, tackling a big project, or just need to bring your A-game, this berry-awesome gummy delivers the same functional kick as our best-selling Energy + Focus shot—now in a tasty chew.
Stress Relief (Cider Crush): Made with a unique blend of botanicals that may help support your body's natural response to stress. Smooth, crisp, and calming—Stress Relief gummies are your go-to for taking the edge off when the pressure's on.
Relax + Unwind (Citrus Chill): Become a Zen master in 20 minutes. When it's time to shut off the noise and reclaim your calm, Relax + Unwind gummies may help you find your peace and bring it with you anywhere.
All formulas feature botanically active ingredients and are available in great-tasting flavors—no harsh aftertaste, just clean, craveable chews that make it easier than ever to Feel Great™.
'Our customers wanted a way to experience the benefits of VIVAZEN without taking a shot,' said Jerry Barker, VP of Innovation at VIVAZEN. 'With these gummies, we've created something that's tasty, portable, and powerful—a new format that fits seamlessly into your daily routine.'
Why fans are loving VIVAZEN Botanical Gummies:
Great new taste: No more compromise—just flavorful, plant-powered goodness.
Convenient packs: Grab-and-go pouches for on-the-move support.
Three functional options: Choose what you need, when you need it.
Try-all variety pack: The perfect intro for new users or gift for your wellness-curious friends.
Whether you're managing stress at work, gearing up for a workout, or just looking for a better way to balance your day, VIVAZEN Botanical Gummies are your new feel-good ritual—plant-based, purpose-driven, and made for real life.
Disclaimer: VIVAZEN products are not intended to diagnose, treat, cure or prevent any disease and these statements have not been evaluated by the FDA.
About VIVAZEN
VIVAZEN fuels Everyday Heroes™ with the power of plants. For over a decade, we've delivered trusted, high-quality botanical supplements that help people power through, focus up, chill out, and boost their mood—without compromise. Rooted in centuries of herbal wisdom and backed by modern innovation, VIVAZEN is a functional, feel-good alternative for those who want to live—and feel—on their own terms. Join the millions who trust VIVAZEN to Feel Great™, naturally and visit https://feelgreatbotanics.com.
SOURCE: VIVAZEN
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Medincell: Half-Year Liquidity Contract Statement
Medincell: Half-Year Liquidity Contract Statement

Business Wire

time2 minutes ago

  • Business Wire

Medincell: Half-Year Liquidity Contract Statement

MONTPELLIER, France--(BUSINESS WIRE)--Regulatory News: Under the liquidity contract entrusted by Medincell (Paris:MEDCL) to Rothschild Martin Maurel, the following resources were included in the liquidity account at June 30, 2025: 5 000 shares 1 145 177 € Over the period from 01/01/2025 to 30/06/2025, a total of : Number of executions Number of shares Traded volume in EUR Buy side 11,807 759,363 11,677,812.97 Sell side 11,343 758,413 11,671,875.50 Expand It should be noted that Medincell increased the funds allocated to the liquidity contract by €600,000 on 11 April 2025. At the time of its implementation on September 11, 2024, the following resources were included in the liquidity account: 8 824 shares 466 568.49 € About Medincell Medincell is a clinical- and commercial-stage biopharmaceutical licensing company developing long-acting injectable drugs in many therapeutic areas. Our innovative treatments aim to guarantee compliance with medical prescriptions, to improve the effectiveness and accessibility of medicines, and to reduce their environmental footprint. They combine active pharmaceutical ingredients with our proprietary BEPO® technology which controls the delivery of a drug at a therapeutic level for several days, weeks or months from the subcutaneous or local injection of a simple deposit of a few millimeters, entirely bioresorbable. The first treatment based on BEPO® technology, intended for the treatment of schizophrenia, was approved by the FDA in April 2023, and is now distributed in the United States by Teva under the name UZEDY® (BEPO® technology is licensed to Teva under the name SteadyTeq™). We collaborate with leading pharmaceutical companies and foundations to improve global health through new treatment options. Based in Montpellier, Medincell currently employs more than 140 people representing more than 25 different nationalities. UZEDY® and SteadyTeq™ are registered trademarks of Teva Pharmaceuticals. This press release may contain forward-looking statements, particularly concerning the progress of the Company's clinical trials. Although the Company considers that its forecasts are based on reasonable assumptions, any statements other than statements of historical fact that may be contained in this press release relating to future events are subject to change without notice, to factors beyond the Company's control and to the Company's financial capabilities. These statements may include, but are not limited to, any statements beginning with, followed by or including words or expressions such as "objective", "believe", "expect", "aim", "intend", "may", "anticipate", "estimate", "plan", "project", "will", "may", "probably", "should", "could" and other words or expressions of similar meaning or used in the negative. Forward-looking statements are subject to inherent risks and uncertainties beyond the Company's control which may cause actual results, performance or achievements of the Company to differ materially from those anticipated or implied by such statements. A list and description of such risks, hazards and uncertainties can be found in the documents filed by the Company with the Autorité des Marchés Financiers (AMF) pursuant to its regulatory obligations, including in the Company's document de base, registered with the AMF on September 4, 2018 under number I. 18-062, as well as in documents and reports to be published subsequently by the Company. Furthermore, these forward-looking statements only apply as of the date of this press release. Readers are cautioned not to place undue reliance on these forward-looking statements. Except as required by law, the Company undertakes no obligation to publicly update these forward-looking statements, nor to update the reasons why actual results may differ materially from those anticipated in the forward-looking statements, even if new information becomes available. The Company's updating of one or more forward-looking statements does not imply that it will or will not update these or any other forward-looking statements. This press release is published for information purposes only. The information contained herein does not constitute an offer to sell or a solicitation of an offer to buy or subscribe for securities of the Company in any jurisdiction whatsoever, particularly in France. Similarly, this press release does not constitute investment advice and should not be treated as such. It is not intended to address the investment objectives, financial situation or specific needs of any particular recipient. It should not be relied upon as a substitute for the exercise of your own judgement. All opinions expressed in this document are subject to change without notice. The distribution of this press release may be restricted by law in certain jurisdictions. Persons into whose possession this press release comes are required to inform themselves about and to observe any such restrictions. 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2,535 23,979.80 40,990.95 28/01/2025 61 135 555 1,555 9,301.80 25,828.55 29/01/2025 254 161 16,266 10,766 269,852.94 177,208.36 30/01/2025 226 230 16,770 16,520 259,767.30 256,060.00 31/01/2025 51 96 1,340 3,188 21,064.80 50,211.00 01/2025 1,989 1,906 84,288 84,436 1,387,432.98 1,390,250.83 03/02/2025 45 95 2,511 2,413 39,046.05 37,811.71 04/02/2025 48 47 2,065 2,065 32,895.45 32,978.05 05/02/2025 45 59 1,100 5,100 17,644.00 82,263.00 06/02/2025 41 39 1,826 1,826 29,928.14 29,946.40 07/02/2025 82 31 3,387 887 54,632.31 14,227.48 10/02/2025 161 69 4,812 2,062 74,537.88 32,167.20 11/02/2025 49 62 3,412 2,512 51,760.04 38,132.16 12/02/2025 52 38 1,643 1,793 24,743.58 27,038.44 13/02/2025 92 80 3,027 1,527 45,072.03 22,843.92 14/02/2025 156 160 4,414 3,414 63,164.34 48,547.08 17/02/2025 91 128 2,886 4,886 41,183.22 69,967.52 18/02/2025 144 95 3,940 3,403 55,238.80 47,744.09 19/02/2025 243 265 12,992 11,529 177,210.88 157,370.85 20/02/2025 245 126 3,818 4,318 52,039.34 59,070.24 21/02/2025 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Target Recall Update Issued Nationwide: Customers Urged Not to Eat Products
Target Recall Update Issued Nationwide: Customers Urged Not to Eat Products

Newsweek

time34 minutes ago

  • Newsweek

Target Recall Update Issued Nationwide: Customers Urged Not to Eat Products

Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources. Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content. Several products stocked at Target stores nationwide have been recalled due to risks ranging from undeclared allergens to potential contamination with Listeria monocytogenes. YoCrunch Yogurts Several types of YoCrunch Yogurts have been recalled by the company due to the potential presence of plastic pieces in the dome topper, which could be a choking hazard if consumed, the Food and Drug Administration said. Out of the products stocked at Target, the affected types are the YoCrunch Low Fat Vanilla with OREO Yogurt, YoCrunch Low Fat Vanilla with M&Ms Yogurt, YoCrunch Low Fat Strawberry with M&Ms Yogurt, all in 4ct/4oz size cups. Also included are the YoCrunch Low Fat Vanilla with OREO and M&Ms Yogurt Variety Pack with 8ct/6oz size cups. The FDA said that the loose plastic pieces are only at risk of being found in the separately packaged topper, and this does not impact the separately packaged yogurt. It said that the transparent plastic pieces may have sharp edges and are between 7 and 25 mm in length. A Target shopping center storefront pictures on Oxon Hill, Maryland USA June 22, 2024. A Target shopping center storefront pictures on Oxon Hill, Maryland USA June 22, 2024. Getty Images Customers who have purchased the affected products are advised not to consume them, and can contact YoCrunch's consumer care department for information about refunds. The recall was initiated voluntarily by manufacturer Danone U.S. in cooperation with the FDA on July 11. Newsweek contacted Danone U.S. for comment via email on Thursday. RITZ Peanut Butter Cracker Sandwiches RITZ Peanut Butter Cracker Sandwiches have been recalled due to incorrect labeling that may not specify they contain peanuts. In several multi-pack varieties, some individual packs may be incorrectly labeled as the cheese variety even though it may be a peanut butter variety, the FDA notice said. All outer labels on cartons are correct. The recall notice said that the issue was a "supplier error" and that corrective actions are being taken to help ensure this issue does not recur. Out of the products stocked at Target, the recall applies to Ritz Cracker Sandwiches with Peanut Butter in the 8ct/11.04oz size, and Ritz Peanut Butter Cracker Sandwiches Family Size 27.6oz/20ct. Customers with peanut allergies are advised to not eat the products and to discard them. The manufacturer Mondelēz Global LLC announced the voluntary recall on July 8. Mondelēz confirmed that it was conducting a voluntary recall of products in an emailed statement to Newsweek and pointed to their press release for more information. Oscar Mayer Turkey Bacon Oscar Mayer Turkey Bacon in 12oz packages sold at Target are among Kraft Heinz products being recalled byb the company due to risks that they are contaminated with Listeria monocytogenes, the United States Department of Agriculture said. The recalled products have the USDA mark of inspection on them. A contamination was detected through lab testing, and no confirmed illnesses have been reported so far. Listeria infection, or listeriosis, can cause severe illness, especially in older adults, those with weakened immune systems, and pregnant women. Symptoms may include fever, muscle aches, and gastrointestinal issues, with more severe risks such as miscarriage and death for vulnerable groups. The USDA urges consumers not to eat the affected turkey bacon and to either discard it or return it to the store. Kraft Heinz told Newsweek in an emailed statement: "We are also working collaboratively with public health authorities, including the United States Department of Agriculture (USDA), to take the appropriate steps and initiate a recall. We deeply regret this situation and apologize to any consumers we have disappointed."

A drug carrying the FDA's most serious warning recalled by a Florida company
A drug carrying the FDA's most serious warning recalled by a Florida company

Miami Herald

timean hour ago

  • Miami Herald

A drug carrying the FDA's most serious warning recalled by a Florida company

A pharmaceutical company based in Naples with research and development division based in Coral Springs recalled a drug for failing an in-house testing of medication degradation. Lupin Pharmaceuticals' Clomipramine Hydrochloride capsules are used 'for the treatment of obsessions and compulsions in patients with Obsessive-Compulsive Disorder (OCD),' according to the National Library of Medicine. The 2,724 recalled 100-count bottles of 25 mg capsules come from lot No. M300464 with an expiration date of June 2025. Lupin issued no press release for the June 27 recall. READ MORE: The role fake Viagra played in a 70-year-old Miami doctor losing his license Clomipramine also counts as an antidepressant and carries an FDA 'Black Box Warning' or 'Boxed Warning' on the packaging that begins: 'Antidepressants increased the risk compared to placebo of suicidal thinking and behavior (suicidality) in children, adolescents, and young adults in short-term studies of major depressive disorder (MDD) and other psychiatric disorders. Anyone considering the use of clomipramine hydrochloride or any other antidepressant in a child, adolescent, or young adult must balance this risk with the clinical need.' If you experience a medical problem because of this or any other drug, first notify a medical professional. Then tell the FDA via the MedWatch program, either online or by calling 800-332-1088.

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