Product Reviews and Information for Epilepsy / Seizure Disorders
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Product Review
CBD Oils, Softgels, Gummies, Creams & Salves Review
See How Much CBD and THC We Found in Products.
Product Review
Coconut Oil and Medium Chain Triglycerides (MCT) Oil Review — Semi-Solid and Liquid Oils & Supplements
Find the Best Coconut Oil and MCT Oil. See How These Oils Compare on Medium Chain Triglycerides (MCTs), Quality, and Value.
Product Review
GABA Supplements Review
Does GABA Work As a Supplement?
CL Answer
Are there drug interactions with magnesium supplements?
Find out about interactions between magnesium supplements and over-the-counter antacids and laxatives such as Maalox, antibiotics, and statins and diabetes medications. ConsumerLab’s answer explains.
CL Answer
Are light boxes effective for preventing and treating seasonal affective disorder (SAD), also known as "winter depression," or circadian rhythm disorders such as jet lag? Which light boxes are best?
Learn about the benefits and safety of light boxes (including who is most likely to benefit), how to use these devices, which commercially available products appear to meet the technical requirements, and who should not use light boxes.
CL Answer
Which supplements may benefit people with essential tremor, and which should be avoided?
Learn about supplements used for treating essential tremor, including caprylic acid (also called octanoic acid), thiamin (vitamin B1), cannabidiol (CBD), GABA (gamma-aminobutyric acid), and branched-chain amino acids. Find out which work and which don't. Also find out which supplements and food may make essential tremors worse.
CL Answer
What is inositol hexaphosphate (IP6) and myo-inositol? Are they helpful in treating cancer or other conditions?
Inositol hexaphosphate (IP6): Find out if IP6 (also known as phytic acid) can prevent or treat cancer. Clinical evidence, dosage, safety and how IP6 differs from myo-inositol. Consumerlab.com's answer explains.
News Release
September 26, 2024
What’s Really In Shilajit Supplements? ConsumerLab Tests Reveal Amounts of Fulvic Acid & Heavy Metals
White Plains, NY, September 26, 2024 -- Shilajit is a tar-like substance created by decomposed plant material and found in mountain rocks.
Recalls & Warnings
December 19, 2024
Gout and Arthritis Supplement Recalled Due to Undeclared Drugs
On December 12, 2024, Buy-herbal recalled all lots of Nhan Sam Tuyet Lien Truy Phong Hoan capsules within expiry after FDA testing found them to contain undeclared furosemide, dexamethasone and chlorpheniramine. These drugs are not permitted in dietary supplements.
Recalls & Warnings
September 24, 2024
Supplement for Eczema Recalled
On September 18, 2024, 123Herbals LLC issued a recall for all lots of Vail-Bon Jie Yang Wan capsules, which are promoted to treat eczema and other skin conditions, because they contain undeclared dexamethasone and chlorpheniramine.
Recalls & Warnings
November 30, 2023
Discover Health, LLC Warned for Promoting CBD Products for Cancer, Epilepsy, & More
On November 16, 2023, the FDA issued a Warning Letter to Discover Health, LLC d/b/a Discover CBD and Strain Snobs following a review of the company’s websites that found statements about the company’s Active CBD Oil – Full Spectrum Distillate Cartridge, Active CBD Oil – ...
Recalls & Warnings
January 18, 2024
FDA Warns Consumers Not to Use Neptune’s Fix Products
On November 21, 2023, the FDA warned consumers not to purchase or use Neptune’s Fix products because they contain tianeptine. The FDA has received severe adverse event reports after use of these products, including seizure and loss of consciousness.
Recalls & Warnings
May 14, 2021
Maker of Care by Design CBD Settles Charges of Unsupported Claims
On May 5, 2021, Cannacraft, Inc.
Recalls & Warnings
July 21, 2022
Young Living Warned for Promoting Essential Oils to Treat Seasonal Allergies, Kidney Stones & More
On June 10, 2022, the FDA issued a warning letter to Young Living Essential Oils Corporate after an inspection of the company’s website and social media found statements about the company’s essential oil and CBD products to be drug claims.
Recalls & Warnings
May 05, 2022
Seller of CBD Tinctures, Creams & Pet Products Promoted for Pain, Cancer & More Warned by FDA
On February 11, 2022, the FDA issued a warning letter to Rena’s Organic following a review of the company’s social media and website, which found statements about the company’s 300 mg CBD Full Spectrum Oil Cannabinoid Tincture, 600 mg CBD Full Spectrum Oil Cannabinoid ...
Recalls & Warnings
April 25, 2020
Injectable Curcumin, CBD Are Not Safe, Warns FDA
On April 9, 2020, the FDA issued a warning letter to BIOTA Biosciences LLC following a review of the company's website, which found statements made about some of the company's, products, including Canabidiol (CBD) Complex, Cannabidiol+Curcumin, and Curcumin Complex to be ...
Recalls & Warnings
April 06, 2022
Mandalorian and Mickey Mouse Hand Sanitizers Recalled Due to Benzene, Methanol
On April 1, 2022, Best Brands Consumer Products, Inc.
News Release
February 23, 2023
Best GABA Supplements Identified by ConsumerLab
White Plains, New York, February 23, 2023 — GABA (gamma-aminobutyric acid) supplements are claimed to have a "calming" effect, and are often promoted to reduce stress and insomnia and improve cognitive performance.
News Release
March 07, 2019
Best Coconut and MCT Oils Identified by ConsumerLab
White Plains, New York, March 7, 2019 — Coconut oil is often promoted as a "healthy fat" and an alternative source of energy to help with weight loss and in conditions such as Alzheimer's disease because it contains medium chain triglycerides (MCTs).
News Release
February 24, 2019
CBD and Collagen Rise in Popularity, as Probiotics and Coconut Oil Dip in Latest ConsumerLab Survey of Supplement Users
White Plains, New York, February 24, 2019 — A recent survey of 10,931 people who use dietary supplements shows that CBD oil (+6.3 percentage points), collagen (+3.6 pts), and bone broth (+2.
Recalls & Warnings
April 03, 2024
FDA Warns Ambaya Gold for Promoting Products for Depression, Cancer, & Arthritis
On December 5, 2023, the FDA issued a Warning Letter to Ambaya Gold Health Products, LLC following review of the company’s website and social media, which found statements about the company’s Brain Balance, Immune System Boost, Dentist In A Bottle, Essensiac, Fulvic Green, Silver ...
Recalls & Warnings
May 08, 2024
APG SEVEN Warned for Promoting Products for Cancer, Depression, Arthritis, & More
On April 18, 2024, the FDA issued a Warning Letter to APG SEVEN, INC following a review of the company’s product labels, website, and social media, which found statements about the company’s BioMoringa, BioDiabetin, Maca Plus, BioProstate, Immune Support, HongoTrap, Honbacterol, ...
Recalls & Warnings
December 01, 2018
Seller of 5-HTP, Potassium & More Warned for Manufacturing Violations
On September 7, 2018, the FDA issued a warning letter to The Delano Company, Inc.
Recalls & Warnings
May 09, 2022
FDA Warns Five Companies for Selling CBD Supplements, Gummies and Creams With Delta-8 THC
On May 4th, 2022, the FDA issued warning letters to five companies for selling CBD and other products labeled as containing delta-8 tetrahydrocannabinol (delta-8 THC).
Recalls & Warnings
April 28, 2020
Natures CBD Oil Distribution Warned for Joint Pain Claims
On April 20, 2020, the FDA issued a warning letter to Homero Corp DBA Natures CBD Oil Distribution, following an inspection of the company's website which found the company's products, including Natures Pure CBD Oil, CBD Froggies 25mg, CBD Froggies 50mg, CBD Edibles 200mg Frogs, CBD ...
Recalls & Warnings
February 22, 2021
FDA Warns Seller of Melatonin & Other Sleep Supplements
On February 18, 2021, the FDA issued a warning letter to SANA Group LLC following a review of the company's website, which found statements made about the company's products Sleep Sana Sleep Drops and Sleep Shots to be drug claims.
Recalls & Warnings
May 23, 2015
Seller of Magnesium, Calcium, Silver and More Warned for Manufacturing Violations, Drug Claims
On May 8, 2015, the FDA issued a warning letter to Pick and Pay, Inc.
Recalls & Warnings
May 24, 2021
U.S. Marshals Seize $1.3 Million Worth of Kratom
U.S. Marshals have seized approximately $1.3 million worth of bulk kratom and kratom supplements manufactured by Atofil, LLC, a subsidiary of Premier Manufacturing Products, according to the FDA.
Recalls & Warnings
August 13, 2016
Seller of Omega-3, Ginkgo, Vision Supplements & More Warned for Drug Claims
On July 22, 2016, the FDA issued a warning letter to Viva Nutraceuticals (J & E International Corporation) following a review of the company's website and promotional literature, which found statement made about its products, Eyestonia, Ginkgo Biloba 60mg, Golden Omega-3 Max, ...
Recalls & Warnings
May 01, 2021
Hand Sanitizer Sold at Ulta, TJ Maxx, and Marshalls Recalled Due to Toxic Chemicals
On April 28, 2021, Scentsational Soaps & Candles, Inc.
Recalls & Warnings
May 08, 2021
FDA Warns Seller of Vitamins B12, C, D, and K
On April 7, 2021, the FDA issued a warning letter to Unived Inc following a review of the company's websites, which found statements made about the company's products Unived brand Colox, CalDveg, B12+D3, and D3+K2-7 to be drug claims.
Recalls & Warnings
February 16, 2021
Seller of BioCBD+ Products Warned for COVID-19 and Drug Claims
On February 11, 2021, the FDA issued a warning letter to Evolved Ayurvedic Discoveries, Inc.
Recalls & Warnings
December 05, 2012
Hydroxycut Class Action Lawsuit To Be Settled
Iovate Health Sciences Inc. has agreed to a settlement of $25.3 million, pending final court approval, in a class action lawsuit that alleged the company deceived consumers about the safety of its Hydroxycut weight loss supplements.
Recalls & Warnings
September 13, 2010
ExtenZe Enhancement Supplements Seized in Canada
On August 19, 2010, Health Canada (Canada's health ministry) seized the sexual enhancement supplements "Male Enhancement ExtenZe" and "Women ExtenZe" which were imported from the U.S. Although legal and widely sold in the U.S.
Recalls & Warnings
October 22, 2002
FDA Seizes Supplements Claiming to Treat Autism
On October 17, 2002 the U.S. Food and Drug Administration (FDA) reported that, at its request, US Marshals seized dietary supplements making drug claims from the Humphrey Laboratories of Lake Oswego, Oregon, doing business as Kirkman Laboratories. U.S.
Recalls & Warnings
February 13, 2016
Cannabis Compound Not Permitted in Supplements, FDA Warns
On February 4, 2016, the FDA issued warning letters to eight companies selling products containing cannabidiol (CBD), a compound derived from cannabis (also known as marijuana). In the U.S., cannabidiol is not permitted to be sold as an ingredient in dietary supplements.
Recalls & Warnings
November 01, 2017
Hemp Oil and Cannabidiol (CBD) Marketers Warned by FDA Over Claims
On November 1, 2017, the FDA announced it issued warning letters to four companies promoting products containing cannabidiol (CBD), a compound derived from cannabis (also known as marijuana), for the treatment of cancer, as well as other diseases, such as Alzheimer's disease. In the U.
Recalls & Warnings
May 01, 2009
FDA Warns Consumers to Stop Using Hydroxycut -- Product Being Tested by ConsumerLab.com
On May 1, 2009, the U.S. Food and Drug Administration warned consumers to immediately stop using Hydroxycut products by Iovate Health Sciences Inc., of Oakville, Ontario and distributed by Iovate Health Sciences USA Inc. of Blasdell, N.Y.
Recalls & Warnings
February 13, 2013
Herbal Supplement Maker Warned For Manufacturing Violations, Misbranding
On February 6, 2013, the FDA issued a warning letter to Genesis Herb Company LLC, following a facility inspection which found the company's Seizure, Relax, Formula ARTH, Disintegrate, Gout, Plantain, and Colloidal Silver dietary supplements to be adulterated because they were prepared, packed, or ...
Recalls & Warnings
July 28, 2008
Seizure of Xiadafil VIP Tablets After Company Refuses Recall
On July 24, 2008, the FDA announced that U.S. Marshals seized nearly $74,000 worth of Xiadafil VIP tablets, Lots 6K029 and 6K209-SEI, distributed by SEI Pharmaceuticals, Inc. of Miami, Fla.
Recalls & Warnings
February 14, 2017
Life Extension Warned for Drug Claims
On February 1, 2017, the FDA issued a warning letter to Life Extension Foundation Buyers Club, Inc.
Recalls & Warnings
October 01, 2016
Homeopathic Teething Tablets and Gels May Pose Danger, FDA Warns
On September 30, 2016, the FDA warned consumers that homeopathic teething tablets and gels may be dangerous for infants and children. The agency has received adverse events reports, including seizures, associated with the use of these products.
Recalls & Warnings
August 15, 2017
Protein Supplements Can Be Dangerous in People with Rare Genetic Disorder
It was recently reported by Yahoo Australian News (August 14, 2017) that a 25-year-old woman died after taking protein supplements and eating protein-rich foods such as lean meats and egg whites in preparation for a fitness competition.
Recalls & Warnings
March 03, 2006
FDA Requests Seizure of More Supplements Containing Ephedrine Alkaloids
On February 24, 2006, the U.S. Food and Drug Administration (FDA) announced that the U.S.
Recalls & Warnings
December 22, 2008
FDA Warns Consumers About Tainted Weight Loss Pills
On December 22, 2008 the U.S. FDA alerted consumers not to purchase or consume any of more than 25 different products marketed for weight loss because they contain undeclared, active pharmaceutical ingredients that may put consumers’ health at risk.
Recalls & Warnings
February 06, 2004
FDA Seizes Ephedra-Containing Dietary Supplements for Unsubstantiated Athletic Performance Claims
On February 5, 2004, Food and Drug Administration Commissioner Mark McClellan, M.D., Ph.D., and U.S. Attorney Michael J. Sullivan announced the seizure of ephedra-containing dietary supplements Betatrim, Thermbuterol, and Stacker 2, from Musclemaster.com in Northboro, Mass.
Recalls & Warnings
January 16, 2014
Joint Health Supplement Contains Dangerous Drugs, FDA Warns
On January 15, 2014, the FDA warned consumers not to buy or use joint health supplement Pro ArthMax (by Human Science Foundation) because it was found to contain multiple drugs, including diclofenac, ibuprofen, naproxen, indomethacin, nefopam, and chlorzoxazone.
Recalls & Warnings
September 02, 2016
Kratom To Be Classified a Schedule I Controlled Substance
On August 30, 2016, the U.S. Drug Enforcement Agency (DEA) announced its intent to classify the active compounds (mitragynine and 7-hydroxymitragynine) in kratom as Schedule I controlled substances.
Recalls & Warnings
January 05, 2005
Marketers of Brain-Rejuvinating Supplement Settle FTC Charges of False Claims
On January 5, 2005, the U.S. Federal Trade Commission (FTC) announced that a company that heavily advertised an herbal dietary supplement called "Sagee" to the Chinese-language and Vietnamese-language communities had settled FTC charges of making false and unsubstantiated claims for the product.
Recalls & Warnings
August 16, 2006
Marketers of Diabetes Supplement Banned From Claiming Products Treat or Cure Diseases
On August 10, 2006, the Federal Trade Commission (FTC) announced that an operation selling Chinese herbal supplements is banned from claiming its products treat or cure diseases, to settle FTC charges it violated a previous court order.
Recalls & Warnings
September 17, 2003
FDA Warns of Illness from Star Anise Teas
On September 10, 2003, the Food and Drug Administration (FDA) advised consumers not to consume "teas" brewed from star anise.
Recalls & Warnings
January 13, 2015
Seller of Speech Disorder Supplement Agrees to Settle FTC Charges of Deceptive Claims
NourishLife, LLC, seller of supplements promoted for treating children's speech disorders, has agreed to pay $200,000 in order to settle FTC charges that claims made on the company's website and in brochures were deceptive and not supported by science.
Recalls & Warnings
June 21, 2011
FDA Seizes Probiotics Over Marketing Claims
On June 7, 2011, the U.S. FDA announced that, at its request, U.S. Marshals seized probiotic products from UAS Laboratories, Inc., of Eden Prairie, Minn. because the company markets the products as drugs.
Recalls & Warnings
April 29, 2012
FDA Says DMAA Can't Be Sold as a Supplement -- Warns Sellers
On April 27, 2012, the U.S.
Recalls & Warnings
March 16, 2006
Garden of Life, Maker of Primal Defense, Settles FTC Charges
On March 9, 2006, The Federal Trade Commission (FTC) announced that an operation that marketed dietary supplements sold at Whole Foods Market, GNC, the Vitamin Shoppe, and on the Internet settled FTC charges that they made deceptive advertising claims about their supplements.
Recalls & Warnings
August 08, 2017
Study Shows Severe Risk in Drinking Hydrogen Peroxide
An analysis of records from the National Poison Data System from a 10-year period ending in 2011 identified 294 reported incidents of people developing adverse symptoms after ingesting 35% (high-concentration) hydrogen peroxide (H202). Among these, 41 (13.
Recalls & Warnings
January 09, 2009
FDA Expands Warning to Consumers About Tainted Weight Loss Pills
On January 8, 2009, the U.S. FDA expanded its nationwide alert to consumers about tainted weight loss pills that contain undeclared, active pharmaceutical ingredients. On December 22, 2008, FDA warned consumers not to purchase or consume 28 different products marketed for weight loss.
Recalls & Warnings
August 31, 2012
Energy, Fat Loss Supplement Recalled For Ephedrine Alkaloids
On August 28, 2012, dietary supplement re-sale distributor Brand New Energy (BNE) issued a recall of EphBurn 25 after FDA testing found the product to contain ephedrine alkaloids.
Recalls & Warnings
October 09, 2013
Use of Chinese Supplement Linked to Rare But Serious Condition
On October 9, 2013, Health Canada warned consumers that Compound Danshen Dripping Pills, manufactured by Tianjin Tasly Pharmaceutical Co., have been associated with a case of methemoglobinemia, a rare but serious condition which may result in coma or death.
Recalls & Warnings
March 04, 2003
U.S. Marshalls Seize Supplements Claiming to Prevent Cancer and Treat Arthritis
On February 12, 2003, at the request of the Food and Drug Administration (FDA), U.S. Marshals seized dietary supplement products from Global Source Management and Consulting, Inc., in Sunrise, Florida. U.S.
Recalls & Warnings
September 10, 2014
Seller of Joint Pain Supplement Warned for Drug Claims
On August 24, 2014, the FDA issued a warning letter to CreAgri, Inc., following a website review, which found statements made about the company's products, including Olivenol plus Easeflex, Olivenol plus Essence Capsules, and Olivenol plus Essence Elixer, to be drug claims.
Recalls & Warnings
April 17, 2018
FDA Warns Seller of Echinacea, Iron, Aloe Supplements & More for Manufacturing Violations
On March 30, 2018, the FDA issued a warning letter to Ozark Country Herbs following a facility inspection which found a number of the company's products, including Echinacea-Goldenseal, Natural Iron, and Aloe-Vera Goldenseal Salve, to be adulterated because they were prepared, packed, or held under ...
Recalls & Warnings
January 26, 2018
Seller of Coenzyme-A Warned For Making Drug Claims
On January 5, 2018, the FDA issued a warning letter to Coenzyme A, Inc. following a facility inspection and review of the company's website that found the company made drug claims about its product Coenzyme-A.
Recalls & Warnings
June 27, 2007
Warning Labels to be Required for Green Tea and Black Cohosh Products
On June 26, 2007, the U.S. Pharmacopeia (USP) Dietary Supplements Information Expert Committee (DSI-EC) voted to require cautionary statements on the labels for green tea extracts and black cohosh dietary supplements.
