US FDA bans 23andme direct to consumer genetic testing kit

FDA Orders Genetic Testing Firm 23andme to Stop Marketing DNA Analysis Service — Blocks Sale of a Company’s Mail-Order Gene Tests – The Food and Drug Administration, USA has ordered 23andme – the maker of a popular genetic-testing kit to stop sales of its heavily marketed product, saying the mail-order tests haven’t been proven effective and could dangerously mislead people about their health.

Better inform consumers about sunscreen to help reduce skin cancer risk, early aging

FDA Announces Changes to Better Inform Consumers About Sunscreen — New Rules Give Consumers More Information to Help Reduce the Risk of Skin Cancer, Early Aging – Sunscreen products meeting modern standards for effectiveness may be labeled with new information to help consumers find products that, when used with other sun protection measures, reduce the risk of skin cancer and early skin aging, as well as help prevent sunburn. The final regulation allows sunscreen products that pass the FDA’s test for protection against both ultraviolet A (UVA) and ultraviolet B (UVB) rays to be labeled as “Broad Spectrum.”

FDA warns consumers not to use skin care products by Clarcon

FDA Warns Consumers Not to Use Skin Products Made by Clarcon Due to Bacterial Contamination Risk – Products marketed under various names. – The U.S. Food and Drug Administration announced that Clarcon Biological Chemistry Laboratory Inc. of Roy, Utah, is voluntarily recalling some skin sanitizers and skin protectants marketed under several different brand names because of high levels of disease-causing bacteria found in the product during a recent inspection.

Consumer group criticizes nyc menu labeling bill

The Center for Consumer Freedom (CCF) criticized the New York City Board of Health for mandating that chain restaurants incorporate nutrition labels on their menus. – The Center for Consumer Freedom (CCF) criticized the New York City Board of Health for mandating that chain restaurants incorporate nutrition labels on their menus. This morning the Board unanimously supported the proposal, even though similar legislation had been previously struck down in court.

Consumer Healthcare supports FDA over OTC cough and cold medicines withdrawal

FDA Bulletin on Kids’ Oral, Over-the-Counter Cough and Cold Reaffirms Industry’s October 2007 Voluntary Withdrawal; Agency announcement reinforces need for increased communication with consumers. – On behalf of the leading makers of over-the-counter (OTC) cough and cold medicines, the Consumer Healthcare Products Association (CHPA) offered its support for U.S. Food and Drug Administration (FDA) decision against the use of oral OTC cough and cold medicines in children under the age of two.

50% Probiotics brand found contaminated with traces of gluten in USA

50% Probiotics brand found contaminated with traces of gluten in USA

New Study Finds that Many Probiotics Are Contaminated with Traces of Gluten – Is my probiotic pack gluten-free? More than half of popular probiotics contain traces of gluten, according to an analysis performed by investigators at the Celiac Disease Center at Columbia University Medical Center (CUMC). Tests on 22 top-selling probiotics revealed that 12 of them (or 55%) had detectable gluten.

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