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Tag: Labeling

FDA Warns Dietary Supplement Firms for Marketing Concussion Treatments

Dietary Supplements, Disease Claims, Drugs, Food, Labeling, Structure-Function Claims, Warning LettersFDA

On September 6, 2012, the U.S. Food and Drug Administration (“FDA”) issued warning letters to two dietary supplement companies in connection with promoting unapproved products as drugs. According to the FDA, the firms cited by the Agency, PruTect Rx and …

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FDA Approves First At-Home HIV Test

FDA, HIV Test, Labeling, Medical Devices, PMAFDA

On July 3, 2012, the U.S. Food and Drug Administration (“FDA”) approved the first over-the-counter (“OTC”) at-home test kit used to detect human immunodeficiency virus (“HIV”). According to the FDA’s announcement, the OraQuick In-Home HIV Test allows the user to …

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FDA Warns Makers of RockStar Coffee & Energy Products

Beverages, Dietary Supplements, Enforcement, Labeling, RockStar, Warning LettersFDA

On May 23, 2012, the U.S. Food and Drug Administration (“FDA”) issued a Warning Letter to the manufacturers of the widely popular RockStar energy products, Rockstar , Inc. (“the Company”). Found here, the Letter contains various allegations that the Company’s …

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Marshals Seize Misbranded Drug Products at Maine Facility per FDA’s Request

Dietary Supplements, Drug Products, Drugs, Enforcement, FDA, Labeling, Warning LettersFDA

On June 6, 2012, the U.S. Food and Drug Administration (“FDA”) announced the seizure of various drug products from a Portland, Maine facility. According to the FDA, U.S. Marshals seized the drug products upon the Agency’s request after it was …

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FDA Releases Draft Guidance Updating Warnings for Labeling of Albumin, Highlighting Risk of Creutzfeldt Jakob Disease

Blood, FDA, Guidance, Labeling, mad cowFDA

On June 11, 2012, the U.S. Food and Drug Administration (“FDA”) published a draft guidance document, entitled Draft Guidance for Industry: Amendment to ‘Guidance for Industry: Revised Preventive Measures to Reduce the Possible Risk of Transmission of Creutzfeldt-Jakob Disease and …

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FDA Alerts Consumers of an Array of Dangers Associated with Reumofan Plus Supplement

Dietary Supplements, Enforcement, FDA, imports, Labeling, Reumofan PlusFDA

On June 1, 2012, the U.S. Food and Drug Administration (“FDA”) issued an alert to consumers on the product Reumofan Plus. Purportedly marketed as a dietary supplement, Reumofan Plus is manufactured in Mexico by the company Riger Naturals. According to …

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FDA and FAAN Aim to Educate Public during Food Allergy Awareness Week

Allergens, FDA, Food, Labeling, Recalls, Warning LettersFDA

This week (May 13 – May 19, 2012) is recognized as Food Allergy Awareness Week (“FAAW”). FAAW was created by the Food Allergy & Anaphylaxis Network (“FAAN”), a non-profit organization dedicated to promoting awareness food allergies and those who suffer …

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FDA Warns of Recall Due to Undeclared Milk Derivatives in Several Beverage Products

Allergens, Beverages, FDA, Food, Labeling, Milk, RecallsFDA

On May 10, 2012, the U.S. Food and Drug Administration (“FDA”) posted a press release on its website notifying consumers of a recent recall of various fruit beverages. Jonlly Fruits Inc., the manufacturer of the beverages, opted to initiate the …

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FDA Explains its Regulation of Bottled Water

Beverages, Bottled Water, CGMP, FDA, LabelingFDA

Recently, the U.S. Food and Drug Administration (“FDA”) published “Food Facts”, a document providing the public with information concerning the Agency’s regulation of bottled water. Found here, the document details how the Agency works in conjunction with the Environmental Protection …

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FDA Approves Drug for Treatment of Plague Through Animal Efficacy Rule

Animal Efficacy, Drugs, FDA, Labeling, NDAFDA

On April 27, 2012, the U.S. Food and Drug Administration (“FDA”) approved Levaquin (levofloxacin), a drug used to treat those afflicted with plague. In addition to treating those with the deadly infection, Levaquin is also approved to reduce the risk …

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    Katherine L. Giannamore
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