Sept. 10, 2021 -- The FDA this week sent informing letters to 10 companies for illegally selling dietary supplements that assertion to cure, treat, oregon prevent diabetes.
The cited products, and the 10 companies that marketplace these products and received the informing letters, are arsenic follows:
- Berry Gen Sugar Control (Live Good Inc.)
- Diabetes Doctor Pre-Diabetes and Diabetes Doctor Blood Sugar 24 Hour (Pharmaganics LLC)
- Lysulin Weight Loss Shake, Lysulin Diabetes and Prediabetes Chewables, Lysulin Diabetes and Prediabetes Liquid, Lysulin Diabetes and Prediabetes Capsules, and Lysulin Diabetes and Prediabetes Powder (Lysulin, Inc.)
- Diabetic Support Formula (Nuturna International LLC)
- GLUCOTYPE2 (Phytag Labs)
- Diabetes Support (Ar-Rahman Pharm LLC)
- DiabetesSupport (Metamune Inc)
- Diabalance Diabetes Supplement (Holistic Healer & Wellness Center Inc.)
- CuraLin (Radhanite LLC, d/b/a CuraLife Ltd)
- Sugar Balance (Aceva LLC)
"More than 34 cardinal Americans -- conscionable implicit 1 successful 10 radical -- are living with diabetes. Dietary supplements that marque fraudulent claims to treat diabetes are unapproved caller drugs that could perchance harm consumers who usage these products alternatively of seeking harmless and effectual FDA-approved treatments,” Cara Welch, PhD, acting manager of the Office of Dietary Supplement Programs successful the FDA’s Center for Food Safety and Applied Nutrition, said successful a statement.
“The FDA is committed to protecting U.S. consumers from products and companies that marque unlawful claims to dainty oregon forestall diabetes, and we’ll proceed to clasp companies accountable by alerting the nationalist astir products that spot consumers astatine risk,” she continued.
Unlike drugs approved by the FDA, the bureau has not evaluated whether the unapproved products taxable to the informing letters are effectual for their intended use, what the due dosage mightiness be, however they could interact with FDA-approved drugs oregon different substances, oregon whether they person unsafe broadside effects oregon different information concerns.
The FDA requested responses from the companies wrong 15 moving days stating however they volition code these issues oregon supply their reasoning and supporting accusation arsenic to wherefore they deliberation the products are not successful usurpation of the law. Failure to close violations promptly whitethorn effect successful ineligible action, including merchandise seizure and/or injunction.
If a user thinks that a merchandise mightiness person caused a absorption oregon an illness, they should halt utilizing the merchandise close distant and interaction their wellness attraction provider. The FDA besides encourages wellness attraction providers and consumers to study adverse reactions associated with FDA-regulated products to the bureau utilizing MedWatch oregon the Safety Reporting Portal.
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