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- Naturade Significantly Strengthens Balance Sheet; Receives $2.5 Million in Capital from Westgate Equity Partners, L.P.
- Natrol Appoints Vincent Andrich VP Sales for Prolab Division
- Vermont Pure Holdings, Ltd. Announces Record Fiscal Year 2001 Results
- Body Shop Reports 24.8 Mil Euro Sales Revenues
- Spectrum Organic Products Responds to FDA Letter Regarding Use of Non-GMO Seal on Canola Oil Label
- Supplement Group Targets Consumer Education
- Advanced Nutraceuticals, Inc. Announces 2001 Year End Results And Additional Financing
- ADM Awarded Nutraceuticals Patent Patent Creates Proprietary Position for ADM in Fast-Growing Nutraceutical Market
- Tantivy Sciences Obtains Exclusive License to Unique Nutraceutical Products
- Top GNC Executives Tour Pittsburgh Market to Present New Business Plan and Expansion Possibilities; Meeting will focus on new business strategies and growth
- Nutrition 21 Receives Patent For the Nutritional Treatment of Type 2 Diabetes; Patent Presents New Pharmaceutical Licensing Opportunities
- ConsumerLab.com Finds Most B-vitamin Supplements Contain What They Claim, But Often Exceed Safe Levels - Consumers Cautioned to Be Aware of Side Effects with High Dose Products
- Nutraceutix, Inc., Nutravite Announcement Commercial Availability of CDT™ Glucosamine for Canadian Marketplace
- Harvey Kamil Appointed President of NBTY, Inc. - Scott Rudolph to Continue as Chairman and CEO
- drugstore.com Expects to Reach Profitability Target in 2003
- Human Genome Project Leads to Innovative Healthcare
- NPIcenter’s Career Center targets nutraceutical Industry
- Adding Vitamin C To Certain Drugs May Help Treat Alzheimer's, Other Brain Disorders
- Adding Vitamin C To Certain Drugs May Help Treat Alzheimer's, Other Brain Disorders
- Editorial: An Exercise in Synergy
- NBTY, Inc. Appoints Harvey Kamil President, Scott Rudolph To Continue As Chairman And CEO
- Ross Products to Launch Infant Formula Supplemented With Two New Fatty Acids
- Ross Products to Launch Infant Formula Supplemented With Two New Fatty Acids
- Ross Products to Launch Infant Formula Supplemented With Two New Fatty Acids
- LignisulMSM vs Naproxen for Osteoarthritis Clinical Trial Gets Underway
- Natural Health Trends Corp. Launches Lexxus Taiwan
- FDA Presents Compliance Guide for Structure/Function Claims
- New TrimFit® Bars Redefine Energy Bar Category
- New TrimFit® Bars Redefine Energy Bar Category
- Probiata® Offers Safe, Natural and Effective Alternative
- Alive & Well with Michelle Harris
- Be Well and Get Rewarded! Find Personalized Wellness Solutions and Earn Free Vitamins at NatureMade.com
- Consumers Search for Healthy Cleaning Products That Work
- Nordic Naturals: Omega 3 Fatty Acids
- Cyanotech Names Bob Capelli as Director of Sales
- CRN Supports "Food Stamp" Bill
Associations, urges committee members to give strong consideration to a bill introduced last week by Senators Tom Harkin (D-Iowa) and Orrin Hatch (R-Utah), that would provide low-income households the opportunity to use their food stamps to purchase vitamin and mineral supplements.
- CRN Supports "Food Stamp" Bill
Associations, urges committee members to give strong consideration to a bill introduced last week by Senators Tom Harkin (D-Iowa) and Orrin Hatch (R-Utah), that would provide low-income households the opportunity to use their food stamps to purchase vitamin and mineral supplements.
- Metafolin ruled safe for use in supplements and foods by JECFA
Company announces that Metafolin, its new patented form of folate, has been approved as a safe alternative to folic acid for use in dietary supplements, foods for special dietary uses and other foods by the Joint FAO/WHO Expert Committee on Food Additives (JECFA).
- Metafolin ruled safe for use in supplements and foods by JECFA
Company announces that Metafolin, its new patented form of folate, has been approved as a safe alternative to folic acid for use in dietary supplements, foods for special dietary uses and other foods by the Joint FAO/WHO Expert Committee on Food Additives (JECFA).
- Metafolin ruled safe for use in supplements and foods by JECFA
Company announces that Metafolin, its new patented form of folate, has been approved as a safe alternative to folic acid for use in dietary supplements, foods for special dietary uses and other foods by the Joint FAO/WHO Expert Committee on Food Additives (JECFA).
- Metafolin ruled safe for use in supplements and foods by JECFA
Company announces that Metafolin, its new patented form of folate, has been approved as a safe alternative to folic acid for use in dietary supplements, foods for special dietary uses and other foods by the Joint FAO/WHO Expert Committee on Food Additives (JECFA).
- Metafolin ruled safe for use in supplements and foods by JECFA
Company announces that Metafolin, its new patented form of folate, has been approved as a safe alternative to folic acid for use in dietary supplements, foods for special dietary uses and other foods by the Joint FAO/WHO Expert Committee on Food Additives (JECFA).
- Metafolin ruled safe for use in supplements and foods by JECFA
Company announces that Metafolin, its new patented form of folate, has been approved as a safe alternative to folic acid for use in dietary supplements, foods for special dietary uses and other foods by the Joint FAO/WHO Expert Committee on Food Additives (JECFA).
- Metafolin ruled safe for use in supplements and foods by JECFA
Company announces that Metafolin, its new patented form of folate, has been approved as a safe alternative to folic acid for use in dietary supplements, foods for special dietary uses and other foods by the Joint FAO/WHO Expert Committee on Food Additives (JECFA).
- Food & Drug Administration approves LycoMato® as safe color additive
FDA is amending its color additive regulations to provide for the safe use of LycoMato® tomato lycopene extract as a color additive in foods, in response to a Color Additive Petition filed by LycoRed Natural Products Industries.
- Food & Drug Administration approves LycoMato® as safe color additive
FDA is amending its color additive regulations to provide for the safe use of LycoMato® tomato lycopene extract as a color additive in foods, in response to a Color Additive Petition filed by LycoRed Natural Products Industries.
- Food & Drug Administration approves LycoMato® as safe color additive
FDA is amending its color additive regulations to provide for the safe use of LycoMato® tomato lycopene extract as a color additive in foods, in response to a Color Additive Petition filed by LycoRed Natural Products Industries.
- Food & Drug Administration approves LycoMato® as safe color additive
FDA is amending its color additive regulations to provide for the safe use of LycoMato® tomato lycopene extract as a color additive in foods, in response to a Color Additive Petition filed by LycoRed Natural Products Industries.
- Food & Drug Administration approves LycoMato® as safe color additive
FDA is amending its color additive regulations to provide for the safe use of LycoMato® tomato lycopene extract as a color additive in foods, in response to a Color Additive Petition filed by LycoRed Natural Products Industries.
- Effective Date of AHPA Trade Recommendations Nears
Recommendations include: appropriate steps be taken to assure that black cohosh rhizome and root raw material is free of its known adulterant, Chinese cimicifuga rhizome and root, and dislosure of caffeine on product labels.
- Effective Date of AHPA Trade Recommendations Nears
Recommendations include: appropriate steps be taken to assure that black cohosh rhizome and root raw material is free of its known adulterant, Chinese cimicifuga rhizome and root, and dislosure of caffeine on product labels.
- Effective Date of AHPA Trade Recommendations Nears
Recommendations include: appropriate steps be taken to assure that black cohosh rhizome and root raw material is free of its known adulterant, Chinese cimicifuga rhizome and root, and dislosure of caffeine on product labels.
- Effective Date of AHPA Trade Recommendations Nears
Recommendations include: appropriate steps be taken to assure that black cohosh rhizome and root raw material is free of its known adulterant, Chinese cimicifuga rhizome and root, and dislosure of caffeine on product labels.
- AHPA Tele-Seminar to Help Companies Understand How FDA Inspections Should be Conducted and Managed
Tele-seminars are scheduled to begin at 2 pm ET / 11 am PT on August 30 and September 8, 2005; each seminar will be limited to just 30 call lines.
- AHPA Tele-Seminar to Help Companies Understand How FDA Inspections Should be Conducted and Managed
Tele-seminars are scheduled to begin at 2 pm ET / 11 am PT on August 30 and September 8, 2005; each seminar will be limited to just 30 call lines.
- FDA Review Period Extended for Nutrition 21's Chromium Picolinate Diabetes-Related Qualified Health Claim Petition
Company agrees to fDA's request to extend review period for two weeks.
- FDA Review Period Extended for Nutrition 21's Chromium Picolinate Diabetes-Related Qualified Health Claim Petition
Company agrees to fDA's request to extend review period for two weeks.
- FDA Approves First Qualified Health Claim for Chromium Picolinate and Risk of Type 2 Diabetes
FDA has concluded that there is credible evidence to support the following qualified health claim: “One small study suggests that chromium picolinate may reduce the risk of insulin resistance, and therefore possibly may reduce the risk of type 2 diabetes. FDA concludes, however, that the existence of such a relationship between chromium picolinate and either insulin resistance or type 2 diabetes is highly uncertain.”
- FDA Approves First Qualified Health Claim for Chromium Picolinate and Risk of Type 2 Diabetes
FDA has concluded that there is credible evidence to support the following qualified health claim: “One small study suggests that chromium picolinate may reduce the risk of insulin resistance, and therefore possibly may reduce the risk of type 2 diabetes. FDA concludes, however, that the existence of such a relationship between chromium picolinate and either insulin resistance or type 2 diabetes is highly uncertain.”
- FDA Approves First Qualified Health Claim for Chromium Picolinate and Risk of Type 2 Diabetes
FDA has concluded that there is credible evidence to support the following qualified health claim: “One small study suggests that chromium picolinate may reduce the risk of insulin resistance, and therefore possibly may reduce the risk of type 2 diabetes. FDA concludes, however, that the existence of such a relationship between chromium picolinate and either insulin resistance or type 2 diabetes is highly uncertain.”
- FDA Approves First Qualified Health Claim for Chromium Picolinate and Risk of Type 2 Diabetes
FDA has concluded that there is credible evidence to support the following qualified health claim: “One small study suggests that chromium picolinate may reduce the risk of insulin resistance, and therefore possibly may reduce the risk of type 2 diabetes. FDA concludes, however, that the existence of such a relationship between chromium picolinate and either insulin resistance or type 2 diabetes is highly uncertain.”
- FDA Publishes Guidance for Bioterrorism Recordkeeping Requirements
FDA announced the publication of a guidance document on the recordkeeping requirements of the Bioterrorism Act; the guidance topics include who must comply with and who is excluded from the rule, and what information is required to be kept and made available to FDA during a Bioterrorism investigation.
- FDA Publishes Guidance for Bioterrorism Recordkeeping Requirements
FDA announced the publication of a guidance document on the recordkeeping requirements of the Bioterrorism Act; the guidance topics include who must comply with and who is excluded from the rule, and what information is required to be kept and made available to FDA during a Bioterrorism investigation.
- NSF International to Host Training Seminar on Good Manufacturing Practices
To help manufacturers interpret the new guidelines, NSF International will be hosting a GMP seminar on October 14, 2005 at the Sheraton Atlantic City Convention Center Hotel in Atlantic City, NJ.
- NSF International to Host Training Seminar on Good Manufacturing Practices
To help manufacturers interpret the new guidelines, NSF International will be hosting a GMP seminar on October 14, 2005 at the Sheraton Atlantic City Convention Center Hotel in Atlantic City, NJ.
- NSF International to Host Training Seminar on Good Manufacturing Practices
To help manufacturers interpret the new guidelines, NSF International will be hosting a GMP seminar on October 14, 2005 at the Sheraton Atlantic City Convention Center Hotel in Atlantic City, NJ.
- NSF International to Host Training Seminar on Good Manufacturing Practices
To help manufacturers interpret the new guidelines, NSF International will be hosting a GMP seminar on October 14, 2005 at the Sheraton Atlantic City Convention Center Hotel in Atlantic City, NJ.
- NSF International to Host Training Seminar on Good Manufacturing Practices
To help manufacturers interpret the new guidelines, NSF International will be hosting a GMP seminar on October 14, 2005 at the Sheraton Atlantic City Convention Center Hotel in Atlantic City, NJ.
- New AHPA FDA Inspection Guidance Available
AHPA’s Guidance for Addressing FDA Inspections of Dietary Supplement Facilities is now available for purchase from AHPA’s online bookstore (http://www.ahpa.org/bookstore.htm).
- New AHPA FDA Inspection Guidance Available
AHPA’s Guidance for Addressing FDA Inspections of Dietary Supplement Facilities is now available for purchase from AHPA’s online bookstore (http://www.ahpa.org/bookstore.htm).
- FDA Commissioner Lester Crawford Resigns
US Food and Drug Administration Commissioner Lester Crawford has announced his resignation effective immediately.
- FDA Commissioner Lester Crawford Resigns
US Food and Drug Administration Commissioner Lester Crawford has announced his resignation effective immediately.
- FDA Commissioner Lester Crawford Resigns
US Food and Drug Administration Commissioner Lester Crawford has announced his resignation effective immediately.
- FDA Commissioner Lester Crawford Resigns
US Food and Drug Administration Commissioner Lester Crawford has announced his resignation effective immediately.
- FDA Commissioner Lester Crawford Resigns
US Food and Drug Administration Commissioner Lester Crawford has announced his resignation effective immediately.
- AHPA Files Further Comments with FDA on NDI Process
Organization's position is that in the case of an unprocessed herb or botanical, a single complete NDI notification is sufficient, but with semi-purified extracts of botanicals, the end product might be significantly different. "“Each manufacturer of such extracts should submit an NDI notification with the requisite safety information.”
- AHPA Files Further Comments with FDA on NDI Process
Organization's position is that in the case of an unprocessed herb or botanical, a single complete NDI notification is sufficient, but with semi-purified extracts of botanicals, the end product might be significantly different. "“Each manufacturer of such extracts should submit an NDI notification with the requisite safety information.”
- Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada
Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient.
- Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada
Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient.
- Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada
Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient.
- Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada
Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient.
- Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada
Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient.
- Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada
Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient.
- Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada
Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient.
- Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada
Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient.
- Developer and Marketers of 'Supreme Greens with MSM' Settle FTC Charges
Supreme Greens developer Alejandro Guerrero and his company, Health Solutions, Inc., and Michael Howell, Gregory Geremesz and their company, Healthy Solutions, LLC have settled Federal Trade Commission charges over their roles in the deceptive marketing of Supreme Greens herbal supplement.
- Developer and Marketers of 'Supreme Greens with MSM' Settle FTC Charges
Supreme Greens developer Alejandro Guerrero and his company, Health Solutions, Inc., and Michael Howell, Gregory Geremesz and their company, Healthy Solutions, LLC have settled Federal Trade Commission charges over their roles in the deceptive marketing of Supreme Greens herbal supplement.
- AHPA Asks FDA, NCCAM to Portray Supplements Honestly
Association challenges the FDA and the National Center for Complementary and Alternative Medicine to tell the truth and to correct past misstatements about dietary supplements and echinacea products, respectively.
- AHPA Asks FDA, NCCAM to Portray Supplements Honestly
Association challenges the FDA and the National Center for Complementary and Alternative Medicine to tell the truth and to correct past misstatements about dietary supplements and echinacea products, respectively.
- AHPA Asks FDA, NCCAM to Portray Supplements Honestly
Association challenges the FDA and the National Center for Complementary and Alternative Medicine to tell the truth and to correct past misstatements about dietary supplements and echinacea products, respectively.
- AHPA Asks FDA, NCCAM to Portray Supplements Honestly
Association challenges the FDA and the National Center for Complementary and Alternative Medicine to tell the truth and to correct past misstatements about dietary supplements and echinacea products, respectively.
- AHPA Asks FDA, NCCAM to Portray Supplements Honestly
Association challenges the FDA and the National Center for Complementary and Alternative Medicine to tell the truth and to correct past misstatements about dietary supplements and echinacea products, respectively.
- AHPA Asks FDA, NCCAM to Portray Supplements Honestly
Association challenges the FDA and the National Center for Complementary and Alternative Medicine to tell the truth and to correct past misstatements about dietary supplements and echinacea products, respectively.
- What Next For Food Supplements In Europe? Conference: Food Supplements in Europe, Challenges for the Future
Government representatives from the food and health sectors of more than twenty EU and non-EU countries met with the European Commission, scientific experts and the food supplement industry in Berlin in September to debate the next stages of development of the regulatory environment for Food Supplements; delegates explored common approaches on the setting of maximum levels for vitamins and minerals, the substantiation of health claims , and potential models for the safety
assessment of ingredients other than vitamins and minerals.
- What Next For Food Supplements In Europe? Conference: Food Supplements in Europe, Challenges for the Future
Government representatives from the food and health sectors of more than twenty EU and non-EU countries met with the European Commission, scientific experts and the food supplement industry in Berlin in September to debate the next stages of development of the regulatory environment for Food Supplements; delegates explored common approaches on the setting of maximum levels for vitamins and minerals, the substantiation of health claims , and potential models for the safety
assessment of ingredients other than vitamins and minerals.
- What Next For Food Supplements In Europe? Conference: Food Supplements in Europe, Challenges for the Future
Government representatives from the food and health sectors of more than twenty EU and non-EU countries met with the European Commission, scientific experts and the food supplement industry in Berlin in September to debate the next stages of development of the regulatory environment for Food Supplements; delegates explored common approaches on the setting of maximum levels for vitamins and minerals, the substantiation of health claims , and potential models for the safety
assessment of ingredients other than vitamins and minerals.
- What Next For Food Supplements In Europe? Conference: Food Supplements in Europe, Challenges for the Future
Government representatives from the food and health sectors of more than twenty EU and non-EU countries met with the European Commission, scientific experts and the food supplement industry in Berlin in September to debate the next stages of development of the regulatory environment for Food Supplements; delegates explored common approaches on the setting of maximum levels for vitamins and minerals, the substantiation of health claims , and potential models for the safety
assessment of ingredients other than vitamins and minerals.
- What Next For Food Supplements In Europe? Conference: Food Supplements in Europe, Challenges for the Future
Government representatives from the food and health sectors of more than twenty EU and non-EU countries met with the European Commission, scientific experts and the food supplement industry in Berlin in September to debate the next stages of development of the regulatory environment for Food Supplements; delegates explored common approaches on the setting of maximum levels for vitamins and minerals, the substantiation of health claims , and potential models for the safety
assessment of ingredients other than vitamins and minerals.
- What Next For Food Supplements In Europe? Conference: Food Supplements in Europe, Challenges for the Future
Government representatives from the food and health sectors of more than twenty EU and non-EU countries met with the European Commission, scientific experts and the food supplement industry in Berlin in September to debate the next stages of development of the regulatory environment for Food Supplements; delegates explored common approaches on the setting of maximum levels for vitamins and minerals, the substantiation of health claims , and potential models for the safety
assessment of ingredients other than vitamins and minerals.
- What Next For Food Supplements In Europe? Conference: Food Supplements in Europe, Challenges for the Future
Government representatives from the food and health sectors of more than twenty EU and non-EU countries met with the European Commission, scientific experts and the food supplement industry in Berlin in September to debate the next stages of development of the regulatory environment for Food Supplements; delegates explored common approaches on the setting of maximum levels for vitamins and minerals, the substantiation of health claims , and potential models for the safety
assessment of ingredients other than vitamins and minerals.
- NBTY, Inc. to Pay $2 Million Penalty For Alleged Violations of FTC Order
Under the terms of a consent decree approved by the Federal Trade Commission, for submission by the U.S. Department of Justice to the federal court for approval, NBTY, Inc. will pay a $2 million civil penalty to settle charges that it violated the terms of a 1995 Commission order by making false and misleading health claims about two of its products - “Royal Tongan Limu" and “Body Success PM Diet Program”.
- NBTY, Inc. to Pay $2 Million Penalty For Alleged Violations of FTC Order
Under the terms of a consent decree approved by the Federal Trade Commission, for submission by the U.S. Department of Justice to the federal court for approval, NBTY, Inc. will pay a $2 million civil penalty to settle charges that it violated the terms of a 1995 Commission order by making false and misleading health claims about two of its products - “Royal Tongan Limu" and “Body Success PM Diet Program”.
- Food Allergen Labeling Law Effective January 1 for All Foods and Dietary Supplements
Any food (including dietary supplements) that contains a major food allergen must include specific warnings when labeled on or after January 1, 2006; AHPA to hold tele-seminar on the new requirement at the end of November, with a repeat session in early December.
- Food Allergen Labeling Law Effective January 1 for All Foods and Dietary Supplements
Any food (including dietary supplements) that contains a major food allergen must include specific warnings when labeled on or after January 1, 2006; AHPA to hold tele-seminar on the new requirement at the end of November, with a repeat session in early December.
- Food Allergen Labeling Law Effective January 1 for All Foods and Dietary Supplements
Any food (including dietary supplements) that contains a major food allergen must include specific warnings when labeled on or after January 1, 2006; AHPA to hold tele-seminar on the new requirement at the end of November, with a repeat session in early December.
- Frost & Sullivan Honours GAT Food Essentials GmbH With European Functional Food & Beverage Microencapsulation Technology Innovation Award
The 2009 Frost & Sullivan European Functional Food & Beverage Microencapsulation Technology Innovation Award has been presented to GAT Food Essentials GmbH in recognition of its proprietary wowCAPS(R) technology.
- Frost & Sullivan Honours GAT Food Essentials GmbH With European Functional Food & Beverage Microencapsulation Technology Innovation Award
The 2009 Frost & Sullivan European Functional Food & Beverage Microencapsulation Technology Innovation Award has been presented to GAT Food Essentials GmbH in recognition of its proprietary wowCAPS(R) technology.
- Frost & Sullivan Honours GAT Food Essentials GmbH With European Functional Food & Beverage Microencapsulation Technology Innovation Award
The 2009 Frost & Sullivan European Functional Food & Beverage Microencapsulation Technology Innovation Award has been presented to GAT Food Essentials GmbH in recognition of its proprietary wowCAPS(R) technology.
- BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates
Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010.
- BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates
Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010.
- BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates
Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010.
- BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates
Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010.
- BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates
Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010.
- BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates
Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010.
- BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates
Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010.
- BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates
Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010.
- BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates
Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010.
- Synergy Flavors Invests in Sensory Flavor Profiling Research
Synergy Flavors has commissioned a new research program at North Carolina State University to study the sensory profiles of a range of protein ingredients.
- Synergy Flavors Invests in Sensory Flavor Profiling Research
Synergy Flavors has commissioned a new research program at North Carolina State University to study the sensory profiles of a range of protein ingredients.
- Synergy Flavors Invests in Sensory Flavor Profiling Research
Synergy Flavors has commissioned a new research program at North Carolina State University to study the sensory profiles of a range of protein ingredients.
- Synergy Flavors Invests in Sensory Flavor Profiling Research
Synergy Flavors has commissioned a new research program at North Carolina State University to study the sensory profiles of a range of protein ingredients.
- Synergy Flavors Invests in Sensory Flavor Profiling Research
Synergy Flavors has commissioned a new research program at North Carolina State University to study the sensory profiles of a range of protein ingredients.
- Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors
Synergy Flavors Inc., has announced their chocolate flavors offer a versatile solution for cocoa reduction and can be used as cocoa extenders.
- Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors
Synergy Flavors Inc., has announced their chocolate flavors offer a versatile solution for cocoa reduction and can be used as cocoa extenders.
- Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors
Synergy Flavors Inc., has announced their chocolate flavors offer a versatile solution for cocoa reduction and can be used as cocoa extenders.
- Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors
Synergy Flavors Inc., has announced their chocolate flavors offer a versatile solution for cocoa reduction and can be used as cocoa extenders.
- Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors
Synergy Flavors Inc., has announced their chocolate flavors offer a versatile solution for cocoa reduction and can be used as cocoa extenders.
- Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors
Synergy Flavors Inc., has announced their chocolate flavors offer a versatile solution for cocoa reduction and can be used as cocoa extenders.
- Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors
Synergy Flavors Inc., has announced their chocolate flavors offer a versatile solution for cocoa reduction and can be used as cocoa extenders.
- NPI Daily - Top of The News for Nov. 20, 2009 - FDA Issues 22 Warning Letters to Website Operators
Frost & Sullivan Honours GAT Food Essentials GmbH With European Functional Food & Beverage Microencapsulation Technology Innovation Award; Synergy Flavors Invests in Sensory Flavor Profiling Research; FDA Issues 22 Warning Letters to Website Operators; Nordic Naturals Ultimate Omega™ First Fish Oil to Participate in NFL/NFLPA Sports Nutrition Label Certification Program; BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates; New Organic Berry Whole Food Energy Bar from Amazing Grass Delivers Whole Food Nutrition; Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors
- NPI Daily - Top of The News for Nov. 20, 2009 - FDA Issues 22 Warning Letters to Website Operators
Frost & Sullivan Honours GAT Food Essentials GmbH With European Functional Food & Beverage Microencapsulation Technology Innovation Award; Synergy Flavors Invests in Sensory Flavor Profiling Research; FDA Issues 22 Warning Letters to Website Operators; Nordic Naturals Ultimate Omega™ First Fish Oil to Participate in NFL/NFLPA Sports Nutrition Label Certification Program; BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates; New Organic Berry Whole Food Energy Bar from Amazing Grass Delivers Whole Food Nutrition; Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors
- Heart Health Alert: Niacin May Reverse Hardening of the Arteries
- Heart Health Alert: Niacin May Reverse Hardening of the Arteries
- Heart Health Alert: Niacin May Reverse Hardening of the Arteries
- Heart Health Alert: Niacin May Reverse Hardening of the Arteries
- Spotlight on Savory Side Dishes
- Spotlight on Savory Side Dishes
- Spotlight on Savory Side Dishes
- Another Reason to Choose Healthy Lifestyle Habits
- Another Reason to Choose Healthy Lifestyle Habits
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FTC’s Litigation Continues Against Four Remaining Defendants
Three defendants will give up $4.5 million in cash and other assets to settle Federal Trade Commission charges stemming from their roles in the marketing of CortiSlim and CortiStress, dietary supplements promoted for weight loss and disease prevention, respectively. The surrendered assets will include an investment partnership and related charitable foundation, a speedboat, a truck, and a variety of real estate interests. As part of the settlement, the defendants cannot seek a cash refund of state or federal taxes for 2003, 2004, or 2005 that were paid prior to the settlement. In its complaint, the FTC alleged that the defendants made false or unsubstantiated product claims and used deceptively formatted infomercials in pitching the dietary supplements.
The defendants in the settlement announced today, California-based Pinnacle Marketing Concepts, Inc. (“Pinnacle”) and its president, Thomas F. Cheng, and Utah-based Shawn M. Talbott, cannot make benefit or efficacy claims for any dietary supplement, food, drug, cosmetic, or device unless the claims are truthful and substantiated. Litigation continues against the four defendants who have not settled.
In September 2004, the Commission filed a complaint against Window Rock Enterprises, Inc.; Stephen F. Cheng; Infinity Advertising, Inc.; Gregory S. Cynaumon; and Shawn M. Talbott. The Commission later amended its complaint to add Pinnacle and Thomas F. Cheng as additional defendants. The FTC alleges that advertising claims about CortiSlim’s ability to, among other things, cause rapid, substantial, and permanent weight loss in all users were false or unsubstantiated, as were claims about CortiStress’s ability to reduce the risk of, or prevent, osteoporosis, obesity, diabetes, Alzheimer’s disease, cancer, and cardiovascular disease. The FTC also alleges that CortiSlim and CortiStress infomercials were deceptively formatted to appear as talk shows rather than advertisements. The advertising campaign for CortiSlim ran nationwide, including ads on broadcast and cable television, radio, print media, and the Internet.
The FTC announced two separate stipulated final agreements and orders for permanent injunction today, one with Pinnacle and its president, Thomas Cheng, who the FTC alleges participated in the marketing of Cortislim and CortiStress; and one with Talbott, who the FTC alleges formulated the two products and participated in the advertising. Both orders prohibit the making of certain claims about CortiSlim and CortiStress and require competent and reliable scientific evidence to support any other claims made about the products. The orders also bar misrepresentations of any tests or studies and prohibit claims about the performance, effects on weight, or other health benefits of any dietary supplement, food, drug, cosmetic, or device unless the claims are true, not misleading, and substantiated by competent and reliable scientific evidence. Finally, both orders prohibit the use of deceptively formatted television and radio advertisements and require the use of “paid advertisement” disclosures for television ads longer than 15 minutes and for radio ads longer than five minutes.
The settlement with Pinnacle and Thomas Cheng requires them to give up $3.4 million in assets: $700,000 cash; the net proceeds from an investment partnership and related charitable foundation; a $215,000 boat; a $40,000 truck; and a $450,000 property lien. If they are later found to have misrepresented their financial status, the two defendants would be liable for a $23.8 million judgment.
The settlement with Talbott requires him to give up $1.12 million in assets: $225,000 cash; $350,000 from equity in property in Centerville, Massachusetts, or title to the property; $38,700 from the sale of a timeshare in Hawaii or title to the timeshare; and cash equal to 80 percent of the current market value of a property in Lisbon, Ohio, or title to the property. If Talbott is later found to have misrepresented his financial status, he would be liable for a $3.5 million judgment.
Under the agreements, the defendants also assign to the FTC all claims they might have against the other defendants in this case, and they will not use their settlement with the Commission as a basis for seeking a cash refund of income taxes that they reported as paid. In addition, the agreements include standard record-keeping provisions and require the defendants to distribute copies of the orders to certain entities and individuals.
The Commission vote to authorize staff to file the stipulated final orders was 4-0. The stipulated final orders for permanent injunction were filed in the U.S. District Court for the Central District of California on September 20, 2005.
NOTE: These stipulated final orders are for settlement purposes only and do not constitute an admission of liability by the defendants. A stipulated final order acquires the force of law when signed by the judge.
Copies of the stipulated final orders are available from the FTC’s Web site at http://www.ftc.gov and also from the FTC’s Consumer Response Center, Room 130, 600 Pennsylvania Avenue, N.W., Washington, D.C. 20580. The FTC works for the consumer to prevent fraudulent, deceptive, and unfair business practices in the marketplace and to provide information to help consumers spot, stop, and avoid them. To file a complaint in English or Spanish (bilingual counselors are available to take complaints), or to get free information on any of 150 consumer topics, call toll-free, 1-877-FTC-HELP (1-877-382-4357), or use the complaint form at http://www.ftc.gov. The FTC enters Internet, telemarketing, identity theft, and other fraud-related complaints into Consumer Sentinel, a secure, online database available to hundreds of civil and criminal law enforcement agencies in the U.S. and abroad. |