Product Reviews and Information for Cavity Prevention
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CL Answer
Here’s What You Should Look For In Toothpaste and Mouthwash, and Our Top Picks
Learn about ingredients you want in your toothpaste, mouthwash and other dental products and which ingredients you may want to avoid.
CL Answer
Is Bottled Water Better Than Tap Water?
Some people consider bottled water to be a favorable alternative to tap water, but is it really better? Find out how bottled water and tap water compare in terms of taste, mineral content, acidity, and contaminants such as microplastics and PFAS.
CL Answer
Can fluoride in toothpaste, mouth rinses or drinking water cause attention-deficit/hyperactivity disorder (ADHD) or other neurodevelopmental disorders in children?
Find out if community water fluoridation increases the risk of attention-deficit/hyperactivity disorder (ADHD) or causes lower IQ in children, and learn what the American Dental Association recommends when using fluoride-containing toothpaste and mouth rinses in children.
CL Answer
How likely are Americans to be deficient in vitamins or minerals?
Read info based on the CDC about vitamin deficiencies such as vitamin A, B-6, B-12, C, D, and E, folate, and iron in the United States.
CL Answer
Are gummy vitamins better or worse than pills?
Learn more about gummy supplements, including those for multivitamins, vitamins C and D, calcium, and B vitamins.
News Release
April 28, 2009
40% of Green Tea and Selenium Products Fail ConsumerLab.com Review of Cancer-Prevention Supplements; Lycopene Supplements Pass
WHITE PLAINS, NEW YORK — APRIL 28, 2009 — ConsumerLab.com announced results today of its Product Review of Supplements for Cancer Prevention. Among the products that ConsumerLab.com selected for testing, quality problems were found with two out of five green tea supplements.
News Release
April 26, 2006
ConsumerLab.com tests cancer-prevention supplements; several contaminated with lead or low in ingredient — Report available for green tea, selenium, and lycopene supplements
WESTCHESTER COUNTY, NEW YORK — APRIL 26, 2006 ConsumerLab.com announced results today from its new Product Review of Supplements for Cancer Prevention covering 22 products. Cancer is the second leading cause of death in the U.S.
Recalls & Warnings
January 03, 2025
Essential Oil Sold on Amazon Recalled
On January 2, 2025, Euqee Wintergreen Essential Oils, sold on Amazon were recalled because the packaging is not child-resistant and may pose a risk of poisoning for young children.
Recalls & Warnings
July 20, 2023
FTC Files Complaint Against Company Promoting “Sobrenix” Supplements for Alcohol Cravings
On July 19, 2023, the FTC filed a complaint against Rejuvica and the company owners for promoting its Sobrenix supplements, which contain ingredients such as vitamin B6, thiamin, milk thistle, Chanca Piedra, and dandelion root, to reduce and eliminate alcohol cravings and consumption.
News Release
May 05, 2002
Study finds supplement users avoid prescription drugs due to side effects, not cost — Brands top rated by users also identified in new survey by ConsumerLab.com
WHITE PLAINS, NY — March 5, 2002 — ConsumerLab.com, traditionally known for its independent laboratory evaluations of dietary supplements and nutritional products, announced surprising findings today from a new survey of supplement users.
News Release
March 06, 2002
Study finds supplement users avoid prescription drugs due to side effects, not cost — Brands top rated by users also identified in new survey by ConsumerLab.com
WHITE PLAINS, NY — March 6, 2002 — ConsumerLab.com, traditionally known for its independent laboratory evaluations of dietary supplements and nutritional products, announced surprising findings today from a new survey of supplement users.
Recalls & Warnings
July 22, 2022
FDA Warns Seller of Vision, Calcium & Magnesium Supplements and More
On June 14, 2022, the FDA issued a warning letter to New Sun Inc. following inspection of the company’s website which found statements about the company’s products to be drug claims.
Recalls & Warnings
April 24, 2024
Organic Basil Sold at Trader Joe’s & Other Markets Recalled Due to Salmonella Risk
On April 18, 2024, Infinite Herbs, LLC issued a recall of certain packages of Infinite Herbs and Melissa’s brand fresh organic basil due to the potential presence of Salmonella.
Recalls & Warnings
June 17, 2024
Do Not Consume Diamond Shruumz Products, Warns CDC and FDA
On June 12, 2024, the Center for Disease Control and Prevention (CDC), Food and Drug Administration (FDA), and America’s Poison Centers warned consumers not to buy or consume Diamond Shruumz chocolate bars, cones, and gummies.
Recalls & Warnings
June 27, 2024
“Authentic” Rose Oil Often Is Not
Damask rose essential oil (Rosa × damascene) and products claiming to contain this oil, or “authentic rose oil” may often be adulterated or contain less expensive oils instead, according to a recent bulletin from the American Botanical Association (ABC).
Recalls & Warnings
April 20, 2021
Chiropractor Who Claimed Vitamin D and Zinc Work Better Than COVID Vaccines Charged by FTC
On April 15, 2021, the FTC charged St.
Recalls & Warnings
December 02, 2020
Seller of Vitamin C, Elderberry, Silver, and More Warned for COVID-19 Claims
On November 10, 2020, the FDA issued a warning letter to Sage Woman Herbs, Ltd.
Recalls & Warnings
December 11, 2020
Colloidal Silver Seller Warned for COVID-19 Claims
On December 2, 2020, the FDA issued a warning letter to Heavenly Natural Products for selling various Carbon 60 and colloidal silver products, including AVOCADO C60 ANTI-VIRAL COMBO — VIRUS PREVENTION (made with C60 WITH AVOCADO and Heavenly Silver) with unsupported ...
Recalls & Warnings
November 28, 2022
Seller of Joint Health, Collagen Protein and More Warned for Drug Claims
On November 14, 2022, the FDA issued a warning letter to The Truth Company, LLC (parent company of Kinobody, LLC and UMZU, LLC) following inspection of the company’s websites which found statements about its Betaine, Immune, Redwood, Sensolin, Thyrite, zuRelief, Kino Aminos, Kino Collagen ...
Recalls & Warnings
December 01, 2022
FTC Takes Action Against Company Promoting “COVID Resist” Supplement to Treat COVID-19
On November 22, 2022, the FTC filed a complaint in a U.S. district court against California-based company Precision Patient Outcomes, Inc. for promoting its COVID Resist and VIRUS Resist supplements to prevent and treat COVID-19.
Recalls & Warnings
December 12, 2022
FDA Warns Saffron USA for Promoting Teas to Treat Insomnia, Osteoporosis & Cancer
On September 23, 2022, the FDA issued a warning letter to Saffron USA LLC following inspection of the company’s website which found statements about its Allergy Blend, Chamomile Tea Petals, Diabetic Support Blend, Orange Blast Tea, and Saffron Loose Tea products to be drug ...
Recalls & Warnings
January 10, 2023
Seller of CBD Warned for COVID-19 Claims
On January 5, 2023, the FDA issued a warning to PharmaCanna after review of the company’s website and social media, which found statements about the company’s cannabidiol (CBD) product, CBDefense 2000, to be drug claims because they promoted the products to prevent or treat ...
Recalls & Warnings
February 06, 2023
Recalled Eye Drops Linked to Vision Loss and One Death
On February 2, 2023, Global Pharma Healthcare issued a nationwide recall of its Artificial Tears Lubricant Eye Drops due to potential contamination with bacteria that can cause serious infection, blindness, and death.
Recalls & Warnings
June 22, 2023
Nationwide Pharmaceutical’s Ferrous Sulfate Supplements Recalled
On June 22, 2023, the U.S.
Recalls & Warnings
February 01, 2022
Complaint Submitted to FTC for doTerra Essential Oil COVID Claims
On January 28, 2022, the website truthinadvertising.org submitted a complaint to the Federal Trade Commission (FTC) against doTerra International, LLC. following a series of Zoom calls from the company titled "Protocols for the Current Climate.
Recalls & Warnings
August 08, 2022
Seller of CBD Warned for COVID-19 Claims
On August 4, 2022, the FDA sent a warning letter to FluxxLab LLC following a review of the company’s website and social media which found statements about the company’s Covid-19 Immune Support Tincture and CBDA+CBD Oil Tincture products to be drug claims because they ...
Recalls & Warnings
April 27, 2022
FDA Warns Manufacturer of Topical Antiseptic Products for COVID Claims
On April 19th, 2022, the FDA issued a warning letter to Kleenhanz, LLC following a review of the company’s website and social media which found statements about the company’s Kleenhanz Towelettes topical antiseptic products to be drug claims.
Recalls & Warnings
February 24, 2022
Seller of Essential Oils Warned for COVID-19 Claims
On February 22, 2022, the FDA issued a warning letter to My Natural Treatment following a review of the company’s website and Facebook page, which found statements about the company’s thyme, black seed, eucalyptus, rosemary, and peppermint oil products to be drug claims.
Recalls & Warnings
May 23, 2013
Seller of Sexual Enhancement, Cholesterol, Resveratrol Supplements and More Warned For Drug Claims
On May 2, 2013, the FDA issued a warning letter to Alternative Health Supplements, following a review of the company's website, which found statements made about several dietary supplements, including Regenerect, Alligin, Astaxanthin Advantage, HDL Cholesterol Management, Resveratrol, Coral Calcium ...
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
July 06, 2021
CBD Products Were Promoted to Treat Cancer and Alzheimer's Without Proof, Says FTC
On July 6, 2021, the Federal Trade Commission (FTC) announced that it has approved a final administrative consent orders against Kushly Industries LLC and the company's owner, Cody Alt, for allegedly making unsupported health claims about its CBD products.
Recalls & Warnings
November 10, 2020
FDA Warns Immusist for Drug Claims
On October 16, 2020, the FDA issued a warning letter to Immusist, LLC following a review of the company's website, which found statements made about the company's products IMMUSIST Original and IMMUSIST Natural to be drug claims.
Recalls & Warnings
February 02, 2021
FDA Warns Seller of Reishi Mushroom Supplements
On January 6, 2021, the FDA issued a warning letter to Entia Biosciences, Inc following a review of the company's website, which found statements made about the company's products Lion's Mane - All Natural Supplement, Antrodia Mushroom Powder, Maitake Mushroom Powder, Reishi ...
Recalls & Warnings
August 10, 2020
Seller Indicted for Promoting Silver Product as Coronavirus Cure
On July 28, 2020, Utah resident Gordon Pedersen was indicted by a federal grand jury for posing as a medical doctor to sell an unapproved treatment for coronavirus (COVID-19).
Recalls & Warnings
July 03, 2020
Seller of "COVID Supplement Protection Pack" Warned for Coronavirus Claims
On June 30, 2020, the FDA issued a warning letter to Center for Wellness and Integrative Medicine for selling the products COVID Supplement Protection Pack (also referred to as the COVID Household Value Pack), Thymosin-Alpha, and Methylene Blue Capsules with unsupported ...
Recalls & Warnings
May 09, 2020
Federal Court Orders Seller to Stop Promoting Silver Product as Coronavirus Cure
On April 29, 2020, a federal court in Utah announced that it has obtained a temporary restraining order preventing Gordon Pedersen and his companies, My Doctor Suggests LLC and GP Silver LLC, from promoting fake treatments for coronavirus (COVID-19).
Recalls & Warnings
April 17, 2020
Earth Angel Oils Warned for Coronavirus Claims
On April 14, 2020, the FDA issued a warning letter to Earth Angel Oils for selling products with unsupported claims that they can treat coronavirus (COVID-19).
Recalls & Warnings
April 14, 2020
Herbs of Kedem Warned for Making Coronavirus Claims
On April 10, 2020, the FDA issued a warning letter to Herbs of Kedem for selling products with unsupported claims that they can treat coronavirus (COVID-19).
Recalls & Warnings
March 09, 2020
FDA Warns Sellers of Essential Oils, Colloidal Silver & Teas Promoted to Treat Coronavirus
On March 9, 2020, the FDA and FTC announced they have issued joint warning letters to seven companies for selling products such as essential oils, teas and colloidal silver with unsupported claims that they can treat coronavirus (COVID-19).
Recalls & Warnings
June 07, 2017
FDA Warns Seller of Probiotic and Omega-3 Supplements for Manufacturing Violations
On May 22, 2017, the FDA issued a warning letter to BioTE Medical, LLC following a facility inspection which found its products, including BioTE DIM, BiotTE Probiotic, BioTE Iodine Plus, and BioTE Omega 3 to be adulterated because they were prepared, packed, or held under ...
Recalls & Warnings
April 12, 2013
Zicam Advised Against Using Cold Prevention Claim In Advertising
On April 5, 2013, it was reported that the National Advertising Division (NAD) recommended that Matrixx Initiatives, maker of Zicam cold products, stop making claims in its advertising that the product can prevent colds.
Recalls & Warnings
January 18, 2013
FTC Upholds Ruling, POM Wonderful Health Claims Were Deceptive
On January 16, 2013, the Federal Trade Commission (FTC) announced it will uphold a judge’s ruling that makers of POM Wonderful 100% Pomegranate Juice and POMx supplements made deceptive and unsubstantiated claims that the products could treat, prevent, or reduce the risk of heart disease, prostate ...
Recalls & Warnings
September 26, 2012
Maker of Eye Health Supplements Warned for Drug Claims
On September 18, 2012, the FDA issued a warning letter to EyeScience Labs, L.L.C. because statements made about the company's Macular Health Formula, Dry Eye Formula and Diabetic Vision Formula supplements were found to constitute drug claims.
Recalls & Warnings
September 10, 2012
Maker of Omega-3, Bone and Brain and Supplements Warned For Drug Claims
On August 27, 2012, the FDA issued a warning letter to PruTect Rx indicating that statements on the company's websites about Omega3PruTect, NeuroPruTect, VitaminD3PruTect and OsteoPruTect constitute drug claims, although the products are not approved drugs.
Recalls & Warnings
September 26, 2014
FDA Warns Seller of Supplements and Chocolate Promoted to Treat Ebola
On September 23, 2014, the FDA issued a warning letter to Natural Solutions Foundation, following a review of the company's websites which found statements made about Silver Sol Nano Silver (also called The Silver Solution) and CBD Organic Dark Chocolate Bars (also called High Potency CBD Hemp Oil) ...
Recalls & Warnings
March 03, 2012
Seller of Cancer Cures Warned by FDA
On February 9, 2012, the U.S. FDA sent a Warning Letter to BioAnue Laboratories, Inc. informing it that its websites at www.tumorx.com, www.cancerx.org, www.hopewelltechnologieslimited.com, and www.vmhe.
Recalls & Warnings
October 15, 2007
US Marshalls Seize Charantea Supplements Promoted for Diabetes, Anemia and Hypertension
At the request of the U.S. Food and Drug Administration (FDA), on October 9, 2007, U.S. Marshals seized approximately $71,000 of goods from FulLife Natural Options, Inc., of Boca Raton, Fla., which marketed and distributed Charantea Ampalaya Capsules and Charantea Ampalaya Tea.
Recalls & Warnings
October 05, 2011
FDA Warns Nature's Rite of Promoting 8 Supplements as Drugs
The FDA published a Warning Letter dated September 19, 2011 to Nature's Rite, LLC stating that the firm’s online promotion of its various supplements for the treatment or prevention of various diseases cause these products to be considered unapproved drugs.
Recalls & Warnings
June 15, 2003
FTC Alleges "Heartbar" Made Deceptive Claims About Effectiveness
On June 12, 2003, the Federal Trade Commission (FTC) announced that Unither Pharma, Inc. and United Therapeutics Corporation have agreed to settle FTC charges that they made deceptive claims in advertising for their HeartBar product.
Recalls & Warnings
October 06, 2006
FDA Warns Mangosteen Juice Maker of Drug Promotions
On September 20, 2006, the U.S. Food and Drug Administration (FDA) sent a Warning Letter to the makers of Xango, a mangosteen juice product. The letter advised that distributors of the product were using brochures making health claims restricted to the promotion of drugs.
Recalls & Warnings
December 17, 2008
Airborne Settles Over False Advertising -- $7 Million to States
On December 17, 2008, the Seattle Times reported that Airborne Health, makers of a top-selling product marketed as a cold prevention and treatment remedy, signed a $7 million settlement to settle false advertising claims leveled by 32 state attorneys general and the District of Columbia.
Recalls & Warnings
October 24, 2012
Garlic Supplement Maker Warned For Misbranding and Drug Claims
On October 10, 2012, the FDA issued a letter to dietary supplement manufacturer Garlic Wise because statements made in a brochure about the company’s Alli-C garlic supplement promote the product as a drug. Alli-C was also found to be misbranded due to inadequate directions for use.
Recalls & Warnings
September 27, 2010
FTC Charges Deceptive Advertising by POM Wonderful
On September 27, 2010, the U.S.
Recalls & Warnings
January 18, 2005
Supplement Maker to Pay over $3.5 Million to Settle Deceptive Advertising Charges for Immune Dietary Supplement
On January 18, 2005, the Federal Trade Commission (FTC), the Orange County (California) District Attorney, and the California State Attorney General announced that they had reached settlements with Body Wise International, Inc.
Recalls & Warnings
March 17, 2004
Marketers of “Focus Factor” and “V-Factor” Fined for Advertising Claims
On March 17 , 2004 the Federal Trade Commission (FTC) reported that the marketers of “Focus Factor,” a dietary supplement that purports to improve concentration, and “V-Factor,” a supplement that purports to enhance sexual performance, have agreed to settle charges that they made numerous ...
Recalls & Warnings
August 14, 2008
Airborne to Pay $30 Million for Deceptive Advertising of Cold Remedy -- Refunds Available
On August 14, 2008, the Federal Trade Commission (FTC) announced that Airborne Health, Inc.
Recalls & Warnings
June 06, 2017
Seller of Vision, Cholesterol, Prostate Supplements and More Warned for Drug Claims
On May 25, 2017, the FDA issued a warning letter to Herbal Doctor Remedies following a facility inspection and review of the company's websites, www.herb-doc.com, www.ChinaSecretMed.com and www.theraherb.
Recalls & Warnings
April 04, 2017
Seller of B Vitamins, Vitamin C, Potassium & More Warned for Manufacturing Violations
On March 24, 2017 the FDA issued a warning letter to The Sanapac Company, Inc.
Recalls & Warnings
February 16, 2017
U.S. Department of Justice Files Permanent Injunction Against Supplement Manufacturer
On February 16, 2017, the United States Department of Justice filed a complaint against Pick and Pay, Inc.
Recalls & Warnings
March 24, 2016
27 Cases of Salmonella Infection Linked to Recalled Garden of Life Organic Shakes
On March 24, 2016, the Center for Disease Control and Prevention (CDC) announced that 27 cases of Salmonella infection, including five which required hospitalization, are now linked to recalled Garden of Life Raw Meal Organic Shake and Meal Replacement products.
Recalls & Warnings
January 26, 2016
Seller of CoQ10, SAM-e, Vitamin D, and More Warned for Manufacturing Violations, Drug Claims
On January 15, 2016, the FDA issued a warning letter to Nutri-Dyn Midwest, Inc., following a facility inspection which found the company's products, including Cardioauxin BP, Zinc Lozenge, Oliver, Pau D'Arco, Petadolex, Chondro Jointaide, Dynagesic, SAMe-200, Gugulipid.
Recalls & Warnings
October 17, 2015
23,000 ER Visits Linked to Supplements: Palpitations, Swallowing Problems, Allergies Common
Approximately 23,000 emergency room visits per year are attributed to adverse events linked to the use dietary supplements, according to a large, long-term study by the FDA and the Centers for Disease Control and Prevention (CDC).
Recalls & Warnings
February 10, 2015
Seller of "Natural" Cough Syrup Warned for Manufacturing Violations, Drug Claims
On January 21, 2015, the FDA issued a warning letter to Fragrance Manufacturing Incorporated, following a facility inspection which found the company's products, including Maty's All Natural Cough Syrup and Maty's All Natural Cough Syrup for Kids, to be adulterated because they ...
Recalls & Warnings
December 10, 2014
Risk of Fungal Infection from Probiotics in People with Weakened Immune System
On December 9, 2014, the FDA warned that supplements containing live bacteria or yeast have the potential to be contaminated with mold, and may pose a risk of potentially deadly fungal infection in immunocompromised persons.
Recalls & Warnings
October 30, 2008
Possible Risk Rather than Benefit Found in Trial of Vitamin E and Selenium for Prostate Cancer
On October 27, 2008 the National Cancer Institute (NCI) announced that men in the Selenium and Vitamin E Cancer Prevention Trial (SELECT) are being told to stop taking their supplements.
Recalls & Warnings
September 12, 2006
U.S. Marshalls Seize Supplements Promoted as Drugs
On September 6, 2005, the U.S. Food and Drug Administration (FDA) announced that, at its request, U.S. Marshals seized quantities of Ellagimax capsules, Coral Max capsules, Coral Max without Iron capsules, and Advanced Arthritis Support capsules distributed by Advantage Nutraceuticals L.L.C.
Recalls & Warnings
March 08, 2007
FTC Files Against Maker of Calcium and Fertility Supplements
On January 29, 2007, the Federal Trade Commission (FTC) announced that it had filed civil contempt charges against Lane Labs, Inc.
Recalls & Warnings
July 15, 2004
Company Stopped by FTC from Claiming to Prevent or Reverse Memory Loss without Evidence
On July 13, 2004, the Federal Trade Commission(FTC) announced that a dietary supplement manufacturer has settled FTC charges that it violated federal law by making unsubstantiated claims that its product, “Senior Moment,” could prevent memory loss and restore memory function in adults.
Recalls & Warnings
May 24, 2002
Recall Update for Portagen Iron Fortified Nutrition Powder
In its May 22, 2002 Enforcement Report, the U.S. FDA reported the completion of the following Class I Food Recall. A Class I recall is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
Recalls & Warnings
March 12, 2002
Recall of Multivitamin Due to Unsafe Bottling For Children
On March 12, 2002, the U.S. Consumer Product Safety Commission (CPSC) announced that Leiner Health Products, of Carson, Calif., in cooperation with CPSC, is voluntarily recalling about 14,000 bottles of dietary supplements containing iron.
Recalls & Warnings
October 09, 2013
FDA Warns Consumers Not to Use OxyElite Pro As It Investigates Link With Hepatitis
On October 8, 2013, the FDA warned consumers not to buy or use USPLabs’ weight loss supplement OxyElite Pro because it has been linked with 24 cases of acute non-viral hepatitis in Hawaii.
Recalls & Warnings
August 30, 2012
FDA Warns of Medical Claims Made For Numerous Chinese Herbal Products
On August 15, 2012, the FDA warned Dragon Herbs that promotional statements made on the company's website constitute drug claims for twenty herbal products, including CardioPro 2000, Cordyceps, Duanwood Reishi, Gynostemma, Ginseng and Astragalus Combination, Dang Gui and Gelatin, Sweet Relief, ...
Recalls & Warnings
August 09, 2012
Makers of Mineral Water Containing Lithium Warned
On July 20, 2012, the FDA issued a warning letter to Lithia Mineral Water, Inc. declaring Lithia mineral water product to be an approved drug following a 2011 facility inspection.
Recalls & Warnings
April 17, 2012
FDA Warns Seller of Diabetes Supplement Marketed with Rx Claims
The FDA has posted a Warning Letter (dated April 4, 2012) to Leaner Living regarding the marketing of its Glycosolve product.
Recalls & Warnings
July 11, 2017
FDA Warns Dr. Carolyn Dean of Drug Claims Made for Magnesium, Calcium & Other Mineral Supplements
On June 27, 2017, the FDA issued a Warning Letter to Dr. Carolyn Dean of New Capstone, Inc.
