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Noni
Find out if there is evidence supporting the health benefits of noni juice. Plus, information about traditional uses for noni (Morinda citrifolia), safety concerns and more.
Noni Review
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Recalls & Warnings
August 07, 2018
FDA Warns Seller of Noni Juice Products
On July 18, 2018, the FDA issued a warning letter to Hawaiian Organic Noni, LLC, following a facility inspection which found statements made on the labels of certain products, including Hawaiian Organic Noni Fruit Leather, Hawaiian Organic Noni Banana Fruit Leather, Hawaiian Organic Noni ...
CL Answer
Is there a risk of liver toxicity with certain supplements?
Find out if there is risk of liver damage from supplements such as green tea, niacin, red yeast rice and vitamin A.
Recalls & Warnings
July 24, 2014
Seller of Noni Juice Products Warned for Manufacturing Violations, Drug Claims
On July 14, 2014, the FDA issued a warning to Noni Connection dba Puna Noni, following a facility inspection which found the company's Puna Noni 100% Pure Hawaiian Noni Fruit Capsules to be adulterated because they were prepared, packed, or held under conditions that violate Current Good ...
Recalls & Warnings
May 29, 2013
Seller of Colloidal Silver, Noni Juice and Noni Supplements Warned For Drug Claims
On May 16, 2013, the FDA issued a warning letter to Matrix Health Products, Inc.
Recalls & Warnings
September 06, 2016
Seller on Noni Juice Warned for Manufacturing Violations, Drug Claims
On August 26, 2016, the FDA issued a warning letter to Healing Noni Co. L.L.C.
CL Answer
Are there any supplements I should avoid when taking acetaminophen (Tylenol)?
Find out if there are any supplements that should be avoided when taking acetaminophen (Tylenol).
Product Review
Mangosteen Juice and Supplements Review Article
What Are the Benefits of Mangosteen Juice and Supplements? Find Out What Mangosteen Can and Cannot Do For Your Health.
CL Answer
My doctor told me to stop taking supplements because my kidney function was low. After stopping, my kidney function returned to normal. Can taking a lot of supplements really damage the kidneys?
Find out which supplements may damage your kidneys. ConsumerLab explores possible kidney side effects of supplements including chromium, creatine, and vitamin C.
Product Review
Fruits, Veggies, and Other Greens Supplements Review (Including Spirulina and Chlorella)
Avoid Lead in Greens, Problems with Pills, and Don't Give Up Eating Whole Foods.
Recalls & Warnings
September 18, 2012
Maker of Noni, Nopal, Blood Sugar and Cholesterol Supplements Warned For Drug Claims, Misbranding, and Manufacturing Violations
On August 27, 2012, the FDA issued a warning letter to Naturavit, Inc. for making statements about dietary supplements Noni Imperial Hawaiian, Garlic and Parsley, Cholestol, Nopal and Diatrin that constitute drug claims.
Recalls & Warnings
August 30, 2012
Supplement Company Warned For Medical Claims and Misbranding Of Omega-3, CoQ10, Noni Juice And More
On July 12, 2012, the FDA issued a warning letter to Alfa Vitamins Laboratories, Inc.
Recalls & Warnings
April 21, 2020
Life Force Warned for Colloidal Silver, Nitric Oxide Claims
On March 27, 2020, the FDA issued a warning letter to Doctor's Signature Sales and Marketing International Corp.
Recalls & Warnings
November 21, 2014
Seller of Silver Supplement Warned for Claiming to Treat Ebola and Other Viruses
On November 19, 2014, the FDA issued a warning letter to LifeSilver.com, following a review of the website, which found statements made about Silver sol to be drug claims.
Recalls & Warnings
September 07, 2002
FDA Sends Warning Letters to Seven Online Supplement Sellers For Therapeutic Claims
On August 27, 2002, the FDA posted seven "Cyber" letters recently issued from its Center for Food Safety and Applied Nutrition (CFSAN) to internet website operators promoting dietary supplement products that claim to diagnose, mitigate, treat, cure, or prevent a specific disease or class of ...
Recalls & Warnings
June 10, 2017
Seller of Prostate, Immune Supplements & More Warned for Manufacturing Violations
On May 25, 2017 the FDA issued a warning letter to The Herbalist, Inc.
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
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
June 06, 2017
Seller of Herbal Supplements Warned for Manufacturing Violations, Drug Claims
On May 25, 2017 the FDA issued a warning letter to Life Rising Corporation, following a facility inspection which found the company's products, including Stomach Regulator, Fang Feng Formula, Skin Regulator, Regulate Liver, Circulation Regulator, Pancreas Support, Lung Regulator, Pure Tea, ...
Recalls & Warnings
May 30, 2017
Seller of Vitamin C, Calcium, Mushroom Supplements and More Warned for Manufacturing Violations
On May 12, 2017 the FDA issued a warning letter to VitaPurity Corporatio.
Recalls & Warnings
May 02, 2017
Seller of Amino Acid Supplements & More Warned for Manufacturing Violations
On April 20, 2017 the FDA issued a warning letter to Naturecom Inc.
Recalls & Warnings
January 11, 2013
Consumers May Be Eligible For Cold, Allergy and Weight Loss Supplement Refunds
On January 7, 2013, the Federal Trade Commission (FTC) announced that consumers who purchased the Iovate Health dietary supplements Accelis, nanoSLIM, Cold MD, Germ MD, or Allergy MD between January 2006 and July 2010 may qualify for a refund.
Recalls & Warnings
June 11, 2015
FDA Warns Maker of Fruit Energy Drinks for Drug Claims
On May 19, 2015, the FDA issued a warning letter to CK Management, Inc. following a facility inspection which found statements made on product labels and websites about Whole5, Fruit of the Spirit and ViaViente "whole food" fruit puree energy drinks to be drug claims.
Recalls & Warnings
June 18, 2016
Antioxidant Supplement Recalled Due to Allergen Risk
On June 17, 2016 GMJ Natural Products Inc. issued a recall of 32 fluid oz. jugs of Jugo Moringa Plus Antioxidant because they contain undeclared whey protein.
Recalls & Warnings
February 28, 2017
Seller of Tea Supplements Warned for Manufacturing Violations
On February 3, 2017, the FDA issued a warning letter to Kumato Labs, following a facility inspection which found the company's products, including CHO WA Tea, COMOXIN IBS Formula and NEMURI Sleep Formula to be adulterated because they were prepared, packed, or held under ...
Recalls & Warnings
October 25, 2016
Seller of Liquid Aloe & Mineral Supplement Warned for Manufacturing Violations
On August 10, 2016, the FDA issued a warning letter to Perfect Source Natural Products Inc.
Recalls & Warnings
November 18, 2011
FDA Warns Maker of Milk Thistle and L-Carnitine Supplements of Serious Violations
The U.S. FDA posted a Warning Letter to CJ Labs (Miami, Florida) dated November 1, 2011 regarding serious violations of Good Manufacting Practices in the production of its Milk Thistle and L-Carnitine supplements.
Recalls & Warnings
June 23, 2017
FDA Warns Seller of Menopause, Sexual Enhancement, Prostate Supplements and More For Manufacturing Violations
On May 26, 2017 the FDA issued a warning letter to Star Health & Beauty LLC, following a facility inspection which found the company's products, including Nu Essentials Royal Jelly Capsules, NuMan Male Enhancement Capsules, Star's Male Potency Tonic, NuGen HP, She Max HP, and V Max ...
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
April 01, 2017
Maker of Prelief, Urinozinc Prostate Health Formula Warned for Manufacturing Violations
On March 16, 2017 the FDA issued a warning letter to DSE Healthcare Solutions, LLC, following a facility inspection which found the company's products, including Prelief and Urinozinc Prostate Health Formula to be adulterated because they were prepared, packed, or held under ...
Recalls & Warnings
October 08, 2016
Seller of Cell Power and Super Silica Warned for Manufacturing Violations, Misbranding
On September 23, 2016, the FDA issued a warning letter to SSO, Inc.
Recalls & Warnings
September 27, 2016
Seller of B Vitamins, Omega-3s and More Warned for Manufacturing Violations, Drug Claims
On September 15, 2016, the FDA issued a warning letter to Positive Power Nutrition, following a facility inspection which found the company's products, including High Energy C-Complex, Positive Vitality, Positive Performance, Positive CardioGuard, B-Complex 100, Positive Essentials, Positive ...
Recalls & Warnings
September 14, 2016
Seller of Aloe, Prostate and Joint Supplements Warned for Manufacturing Violations
On April 8, 2016, the FDA issued a warning letter to Salud Natural Entrepreneurs, Inc.
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
February 07, 2017
Seller of Chinese Herbal Products for Prostate, Menopause and More Warned for Manufacturing Violations
On January 23, 2017, the FDA issued a warning letter to Herbal Sciences International, Inc.
Recalls & Warnings
January 21, 2017
Seller of "Cancer Kits," Alpha Lipoic Acid Supplements and More Warned for Drug Claims
On December 22, 2016, the FDA issued a warning letter to Northern Health Products, Inc. following a review of the company's websites, www.northernhealthproducts.com and www.petdca.
Recalls & Warnings
January 17, 2017
Seller of Heart, Senior and Teen Supplements Warned For Drug Claims
On December 7, 2016, the FDA issued a warning letter to Esteem Products Ltd following a review of the company's website, which found statements made about its products, Cardio Life, Total Man, Total Woman, Senior Total Man, Senior Total Woman , and Total Teen to be drug ...
Recalls & Warnings
January 07, 2017
Seller of Protein and Workout Supplements Warned for Manufacturing Violations, Label Errors
On December 22, 2016, the FDA issued a warning letter to Rock Solid Nutrition, LLC, following a facility inspection which found the company's products, including Whey Isolate (Cinnabun flavor), Pre-Pump (Massive Mango flavor) and Strength Test to be adulterated because ...
Recalls & Warnings
November 29, 2016
Seller of Mineral, Joint Supplements and More Warned for Manufacturing Violations, Drug Claims
On July 1, 2016, the FDA issued a warning letter to BioGenyx-Basic Reset, following a facility inspection which found the company's products, including Ionyte, Aqualyte, Beta Factor, Bee Gold and Primo Java to be adulterated because they were prepared, packed, or held under ...
Recalls & Warnings
July 26, 2014
Marketers of Nopal Cactus Drink Settle FTC Charges of Deceptive Claims
TriVita Inc., and marketers of the company's "prickly pear" fruit drink Nopalea have agreed to pay $3.5 million in consumer refunds to settle FTC charges they made deceptive claims that the drink treats health problems ranging from skin conditions to joint pain and respiratory problems.
Recalls & Warnings
December 21, 2016
Seller of 5-HTP, Chromium, Curcumin and More Warned for Drug Claims
On December 1, 2016, the FDA issued a warning letter to Aurora Health and Nutrition following a review of the company's website, which found statements made about its products, 5-HTP, Alpha Lipoic Acid, the Argentyn 23 product line, Artecin 90 Vegetarian Capsules, ...
Recalls & Warnings
November 06, 2014
Seller of Cholesterol, Arthritis Supplements and More Warned for Drug Claims
On October 17, 2014, the FDA issued a warning letter to Vitamins Direct (USA) and Golden Pride, Inc., which distribute Flexezy and Physician's Signature brands of dietary supplements, following a facility inspection which found statements made about certain supplements to be drug claims.
Recalls & Warnings
March 13, 2020
FDA Finds Problems at 52% of Supplement Manufacturing Sites in U.S. and 42% Abroad
ConsumerLab.com has obtained results of the FDA's inspections in Fiscal Year 2019 (October 1, 2018 - September 30, 2019) of 598 dietary supplement manufacturing facilities in the U.S.
