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Hydroxycut is a brand of dietary supplements that is marketed as a weight loss aid. Hydroxycut was originally developed and manufactured by MuscleTech Research and Development; MuscleTech was sold to Iovate Health Sciences in 2003–2004 and declared bankruptcy in 2005; Iovate continues to use MuscleTech as a brand to market Hydroxycut.
Pro Clinical Hydroxycut- Tablet form supplement containing the standard formula that can help you lose weight when combined with diet and exercise to be taken approximately 30 minutes before each meal. Hydroxycut Caffeine Free- Tablet form supplement contains the same key weight loss ingredients as Pro Clinical Hydroxycut, but caffeine free.
FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.
In January 2002, Health Canada issued a voluntary recall of all ephedrine products containing more than 8 mg per dose, all combinations of ephedrine with other stimulants such as caffeine, and all ephedrine products marketed for weight-loss or bodybuilding indications, citing a serious risk to health.
TO: File, NDA 20-272 Supplements SE1-036 [Note: This memo should be filed with the December 19, 2003 original submission of this NDA and likewise filed with 20-588/SE1-024 and 21-444/SE1-008.] 1.0 BACKGROUND Autistic Disorder (autism) is a syndrome of mental retardation that begins in early childhood and persists throughout life.
There are 27 eye drops that might cause you to go blind, FDA says. Here are the products consumers should avoid.
A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall.
Consumers who may have bought the recalled products or who have questions can contact SunFed's recall hotline at (888) 542-5849, Monday through Friday from 8 a.m. to 5 p.m. Mountain Time.