Home
- 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
- Comment Period for Traditional Medicine Model Extended
The draft document, “A Proposed Regulatory Model for Traditional Medicines: Guiding Assumptions and Key Components,” was released by the Traditional Medicines (TM) Congress, made up of nine national organizations, last November, with at least 70 comments received to date.
- UK Food Standards Agency board Discusses Folate and Health
Food Standards Agency (FSA) Board today agreed to consult on options for improving the folate status of young women; options include voluntary or mandatory fortification.
- UK Food Standards Agency board Discusses Folate and Health
Food Standards Agency (FSA) Board today agreed to consult on options for improving the folate status of young women; options include voluntary or mandatory fortification.
- UK Food Standards Agency board Discusses Folate and Health
Food Standards Agency (FSA) Board today agreed to consult on options for improving the folate status of young women; options include voluntary or mandatory fortification.
- UK Food Standards Agency board Discusses Folate and Health
Food Standards Agency (FSA) Board today agreed to consult on options for improving the folate status of young women; options include voluntary or mandatory fortification.
- UK Food Standards Agency board Discusses Folate and Health
Food Standards Agency (FSA) Board today agreed to consult on options for improving the folate status of young women; options include voluntary or mandatory fortification.
- Statement by the National Nutritional Foods Association Regarding Today’s Introduction of Child Nutrition Promotion and School Lunch Protection Act in the Senate and House
The National Nutritional Foods Association (NNFA) commends Sen. Tom Harkin (D-Iowa), Reps. Christopher Shays (R-Conn.) and Lynn Woolsey (D-Calif.), and co-sponsors, for introducing legislation addressing important issues pertaining to the health and nutrition of America’s children who rely on schools to provide nutritional and balanced foods as major components of a healthy, daily diet.
- Statement by the National Nutritional Foods Association Regarding Today’s Introduction of Child Nutrition Promotion and School Lunch Protection Act in the Senate and House
The National Nutritional Foods Association (NNFA) commends Sen. Tom Harkin (D-Iowa), Reps. Christopher Shays (R-Conn.) and Lynn Woolsey (D-Calif.), and co-sponsors, for introducing legislation addressing important issues pertaining to the health and nutrition of America’s children who rely on schools to provide nutritional and balanced foods as major components of a healthy, daily diet.
- Natural Health Products Directorate Advises Not to Label Products as 'NPN Pending'
Canada's Natural Health Products Directorate (NHPD) has issued a bulletin advising companies with products awaiting evaluation for product licenses not to label products these products with language describing the status as 'NPN Pending'.
- Natural Health Products Directorate Advises Not to Label Products as 'NPN Pending'
Canada's Natural Health Products Directorate (NHPD) has issued a bulletin advising companies with products awaiting evaluation for product licenses not to label products these products with language describing the status as 'NPN Pending'.
- CRN 2006 Lobby Day
This year’s event included visits with 40 different House and Senate offices, including meetings with Sen. Orrin Hatch (R-UT), Sen. Dick Durbin (D-IL), Rep. Chris Cannon (R-UT), Rep. Mary Bono (R-CA) and Rep. Frank Pallone (D-NJ).
- CRN 2006 Lobby Day
This year’s event included visits with 40 different House and Senate offices, including meetings with Sen. Orrin Hatch (R-UT), Sen. Dick Durbin (D-IL), Rep. Chris Cannon (R-UT), Rep. Mary Bono (R-CA) and Rep. Frank Pallone (D-NJ).
- CRN 2006 Lobby Day
This year’s event included visits with 40 different House and Senate offices, including meetings with Sen. Orrin Hatch (R-UT), Sen. Dick Durbin (D-IL), Rep. Chris Cannon (R-UT), Rep. Mary Bono (R-CA) and Rep. Frank Pallone (D-NJ).
- CRN 2006 Lobby Day
This year’s event included visits with 40 different House and Senate offices, including meetings with Sen. Orrin Hatch (R-UT), Sen. Dick Durbin (D-IL), Rep. Chris Cannon (R-UT), Rep. Mary Bono (R-CA) and Rep. Frank Pallone (D-NJ).
- NHPD Issues April Communiqué
Health Canada's Natural Health Products Directorate (NHPD) has issued its April monthly Communiqué highlighting the announcement from earlier this week that the use of 'NPN Pending' on product labels is prohibited and noting other changes in risk categories and priority dates.
- NHPD Issues April Communiqué
Health Canada's Natural Health Products Directorate (NHPD) has issued its April monthly Communiqué highlighting the announcement from earlier this week that the use of 'NPN Pending' on product labels is prohibited and noting other changes in risk categories and priority dates.
- Natural Health Products Directorate Places Food and Drink Format Product License Applications on Hold
Canada's Natural Health Products Directorate, currently facing a backlog of over 10,000 product license applications, has placed all those products in a food or drink format on hold pending branch level review between the Natural Health Products Directorate and the Foods Directorate to determine under which category these products should be evaluated.
- Natural Health Products Directorate Places Food and Drink Format Product License Applications on Hold
Canada's Natural Health Products Directorate, currently facing a backlog of over 10,000 product license applications, has placed all those products in a food or drink format on hold pending branch level review between the Natural Health Products Directorate and the Foods Directorate to determine under which category these products should be evaluated.
- Natural Health Products Directorate Places Food and Drink Format Product License Applications on Hold
Canada's Natural Health Products Directorate, currently facing a backlog of over 10,000 product license applications, has placed all those products in a food or drink format on hold pending branch level review between the Natural Health Products Directorate and the Foods Directorate to determine under which category these products should be evaluated.
- Natural Health Products Directorate Places Food and Drink Format Product License Applications on Hold
Canada's Natural Health Products Directorate, currently facing a backlog of over 10,000 product license applications, has placed all those products in a food or drink format on hold pending branch level review between the Natural Health Products Directorate and the Foods Directorate to determine under which category these products should be evaluated.
- Natural Health Products Directorate Places Food and Drink Format Product License Applications on Hold
Canada's Natural Health Products Directorate, currently facing a backlog of over 10,000 product license applications, has placed all those products in a food or drink format on hold pending branch level review between the Natural Health Products Directorate and the Foods Directorate to determine under which category these products should be evaluated.
- Excellent Source Claim Allowed For Foods Containing Both EPA and DHA
Company announces the allowance of their petition for an Excellent Source Nutrient Content Claim for foods containing both EPA (Eicosapentaenoic Acid) and DHA (Docosahexaenoic Acid) under the authoritative statement provisions of the Food and Drug Modernization Act (FDAMA).
- Excellent Source Claim Allowed For Foods Containing Both EPA and DHA
Company announces the allowance of their petition for an Excellent Source Nutrient Content Claim for foods containing both EPA (Eicosapentaenoic Acid) and DHA (Docosahexaenoic Acid) under the authoritative statement provisions of the Food and Drug Modernization Act (FDAMA).
- Excellent Source Claim Allowed For Foods Containing Both EPA and DHA
Company announces the allowance of their petition for an Excellent Source Nutrient Content Claim for foods containing both EPA (Eicosapentaenoic Acid) and DHA (Docosahexaenoic Acid) under the authoritative statement provisions of the Food and Drug Modernization Act (FDAMA).
- Excellent Source Claim Allowed For Foods Containing Both EPA and DHA
Company announces the allowance of their petition for an Excellent Source Nutrient Content Claim for foods containing both EPA (Eicosapentaenoic Acid) and DHA (Docosahexaenoic Acid) under the authoritative statement provisions of the Food and Drug Modernization Act (FDAMA).
- CV Technologies Receives FDA Clearance to Sell COLD-fX'R' as a New Dietary Ingredient in U.S.
Company announces that the unique patented active ingredient of the company's COLD-fX (CVT-E002) product has been accepted by the FDA as a New Dietary Ingredient (NDI).
- CV Technologies Receives FDA Clearance to Sell COLD-fX'R' as a New Dietary Ingredient in U.S.
Company announces that the unique patented active ingredient of the company's COLD-fX (CVT-E002) product has been accepted by the FDA as a New Dietary Ingredient (NDI).
- CV Technologies Receives FDA Clearance to Sell COLD-fX'R' as a New Dietary Ingredient in U.S.
Company announces that the unique patented active ingredient of the company's COLD-fX (CVT-E002) product has been accepted by the FDA as a New Dietary Ingredient (NDI).
- CV Technologies Receives FDA Clearance to Sell COLD-fX'R' as a New Dietary Ingredient in U.S.
Company announces that the unique patented active ingredient of the company's COLD-fX (CVT-E002) product has been accepted by the FDA as a New Dietary Ingredient (NDI).
- Malaysian Health Authorities Grant Soy Protein Heart Claim
Malaysian authorities have ruled its nation's food manufacturers can claim foods containing soy protein help reduce a person's cholesterol.
- Malaysian Health Authorities Grant Soy Protein Heart Claim
Malaysian authorities have ruled its nation's food manufacturers can claim foods containing soy protein help reduce a person's cholesterol.
- Malaysian Health Authorities Grant Soy Protein Heart Claim
Malaysian authorities have ruled its nation's food manufacturers can claim foods containing soy protein help reduce a person's cholesterol.
- HHS/FDA on cGMPs: December 2006
The Department of Health and Human Services has forecast a date of December 2006 for the publication by the Food and Drug Administration of a final rule for current good manufacturing practice (cGMP) for dietary supplements. This projection was included in that department’s semiannual regulatory agenda of “potential rule-making” published in the Federal Register on April 24.
- HHS/FDA on cGMPs: December 2006
The Department of Health and Human Services has forecast a date of December 2006 for the publication by the Food and Drug Administration of a final rule for current good manufacturing practice (cGMP) for dietary supplements. This projection was included in that department’s semiannual regulatory agenda of “potential rule-making” published in the Federal Register on April 24.
- HHS/FDA on cGMPs: December 2006
The Department of Health and Human Services has forecast a date of December 2006 for the publication by the Food and Drug Administration of a final rule for current good manufacturing practice (cGMP) for dietary supplements. This projection was included in that department’s semiannual regulatory agenda of “potential rule-making” published in the Federal Register on April 24.
- AHPA NDI Tele-Seminar Includes Essential Guidance Documents, NDI Database Subscription Discounts
This week’s tele-seminar, Navigating FDA’s New Dietary Ingredient Notification Requirements, (May 19, 2006) will premiere the American Herbal Product Association's new Interim Guidance for New Dietary Ingredient Notifications for Manufacturers or Distributors of New Dietary Ingredients.
- AHPA NDI Tele-Seminar Includes Essential Guidance Documents, NDI Database Subscription Discounts
This week’s tele-seminar, Navigating FDA’s New Dietary Ingredient Notification Requirements, (May 19, 2006) will premiere the American Herbal Product Association's new Interim Guidance for New Dietary Ingredient Notifications for Manufacturers or Distributors of New Dietary Ingredients.
- AHPA NDI Tele-Seminar Includes Essential Guidance Documents, NDI Database Subscription Discounts
This week’s tele-seminar, Navigating FDA’s New Dietary Ingredient Notification Requirements, (May 19, 2006) will premiere the American Herbal Product Association's new Interim Guidance for New Dietary Ingredient Notifications for Manufacturers or Distributors of New Dietary Ingredients.
- AHPA NDI Tele-Seminar Includes Essential Guidance Documents, NDI Database Subscription Discounts
This week’s tele-seminar, Navigating FDA’s New Dietary Ingredient Notification Requirements, (May 19, 2006) will premiere the American Herbal Product Association's new Interim Guidance for New Dietary Ingredient Notifications for Manufacturers or Distributors of New Dietary Ingredients.
- CRN Responds To Panel Report On Multivitamins
Organization responds to the report presented by the scientific panel at the NIH State-of-the-Science Conference on Multivitamin/Mineral Supplements and Chronic Disease Prevention held this week in Bethesda, Md.
- CRN Responds To Panel Report On Multivitamins
Organization responds to the report presented by the scientific panel at the NIH State-of-the-Science Conference on Multivitamin/Mineral Supplements and Chronic Disease Prevention held this week in Bethesda, Md.
- European Parliament Passes Second Reading on Health and Nutrition Claims
The European Parliament has passed second reading of the Health and Nutrition Claims Regulation which will govern permitted health and nutrition claims allowable in the European Union. The regulations, incorporating compromise amendments introduced prior to this reading, are expected to be formally adopted by this autumn. The regulation includes strict conditions for nutrition claims, an initial positive list of approved health claims (after which claims submitted will have to be reviewed by the European Food Safety Authority (EFSA) and then approved by the Commission and Member States), and the use of new health claims or disease reduction claims will require specific authorization after scientific assessment and verification.
- European Parliament Passes Second Reading on Health and Nutrition Claims
The European Parliament has passed second reading of the Health and Nutrition Claims Regulation which will govern permitted health and nutrition claims allowable in the European Union. The regulations, incorporating compromise amendments introduced prior to this reading, are expected to be formally adopted by this autumn. The regulation includes strict conditions for nutrition claims, an initial positive list of approved health claims (after which claims submitted will have to be reviewed by the European Food Safety Authority (EFSA) and then approved by the Commission and Member States), and the use of new health claims or disease reduction claims will require specific authorization after scientific assessment and verification.
- European Parliament Passes Second Reading on Health and Nutrition Claims
The European Parliament has passed second reading of the Health and Nutrition Claims Regulation which will govern permitted health and nutrition claims allowable in the European Union. The regulations, incorporating compromise amendments introduced prior to this reading, are expected to be formally adopted by this autumn. The regulation includes strict conditions for nutrition claims, an initial positive list of approved health claims (after which claims submitted will have to be reviewed by the European Food Safety Authority (EFSA) and then approved by the Commission and Member States), and the use of new health claims or disease reduction claims will require specific authorization after scientific assessment and verification.
- European Parliament Passes Second Reading on Health and Nutrition Claims
The European Parliament has passed second reading of the Health and Nutrition Claims Regulation which will govern permitted health and nutrition claims allowable in the European Union. The regulations, incorporating compromise amendments introduced prior to this reading, are expected to be formally adopted by this autumn. The regulation includes strict conditions for nutrition claims, an initial positive list of approved health claims (after which claims submitted will have to be reviewed by the European Food Safety Authority (EFSA) and then approved by the Commission and Member States), and the use of new health claims or disease reduction claims will require specific authorization after scientific assessment and verification.
- European Parliament Passes Second Reading on Health and Nutrition Claims
The European Parliament has passed second reading of the Health and Nutrition Claims Regulation which will govern permitted health and nutrition claims allowable in the European Union. The regulations, incorporating compromise amendments introduced prior to this reading, are expected to be formally adopted by this autumn. The regulation includes strict conditions for nutrition claims, an initial positive list of approved health claims (after which claims submitted will have to be reviewed by the European Food Safety Authority (EFSA) and then approved by the Commission and Member States), and the use of new health claims or disease reduction claims will require specific authorization after scientific assessment and verification.
- European Parliament Passes Second Reading on Health and Nutrition Claims
The European Parliament has passed second reading of the Health and Nutrition Claims Regulation which will govern permitted health and nutrition claims allowable in the European Union. The regulations, incorporating compromise amendments introduced prior to this reading, are expected to be formally adopted by this autumn. The regulation includes strict conditions for nutrition claims, an initial positive list of approved health claims (after which claims submitted will have to be reviewed by the European Food Safety Authority (EFSA) and then approved by the Commission and Member States), and the use of new health claims or disease reduction claims will require specific authorization after scientific assessment and verification.
- European Parliament Passes Second Reading on Health and Nutrition Claims
The European Parliament has passed second reading of the Health and Nutrition Claims Regulation which will govern permitted health and nutrition claims allowable in the European Union. The regulations, incorporating compromise amendments introduced prior to this reading, are expected to be formally adopted by this autumn. The regulation includes strict conditions for nutrition claims, an initial positive list of approved health claims (after which claims submitted will have to be reviewed by the European Food Safety Authority (EFSA) and then approved by the Commission and Member States), and the use of new health claims or disease reduction claims will require specific authorization after scientific assessment and verification.
- European Parliament Passes Second Reading On Fortified Foods Regulations
The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
- European Parliament Passes Second Reading On Fortified Foods Regulations
The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
- European Parliament Passes Second Reading On Fortified Foods Regulations
The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
- European Parliament Passes Second Reading On Fortified Foods Regulations
The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
- European Parliament Passes Second Reading On Fortified Foods Regulations
The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
- European Parliament Passes Second Reading On Fortified Foods Regulations
The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
- European Parliament Passes Second Reading On Fortified Foods Regulations
The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
- Sageant Leads Grassroots Response to FTC Rule That Threatens Network Marketing
Sageant has launched a national grassroots campaign to secure responses to the recently proposed Federal Trade Commission (FTC) new rule on business opportunities.
- Sageant Leads Grassroots Response to FTC Rule That Threatens Network Marketing
Sageant has launched a national grassroots campaign to secure responses to the recently proposed Federal Trade Commission (FTC) new rule on business opportunities.
- NNFA Statement in Response to NIH State-of-the-Science Conference on Multivitamin/Mineral Supplements
In response to findings by the State-of-the-Science Conference on Multivitamin/Mineral Supplements and Chronic Disease Prevention, the National Nutritional Foods Association (NNFA) maintains that multivitamins and other mineral supplements taken by more than 100 million Americans daily are a safe, affordable and effective way to maintain a healthy lifestyle.
- NNFA Statement in Response to NIH State-of-the-Science Conference on Multivitamin/Mineral Supplements
In response to findings by the State-of-the-Science Conference on Multivitamin/Mineral Supplements and Chronic Disease Prevention, the National Nutritional Foods Association (NNFA) maintains that multivitamins and other mineral supplements taken by more than 100 million Americans daily are a safe, affordable and effective way to maintain a healthy lifestyle.
- NNFA Statement in Response to NIH State-of-the-Science Conference on Multivitamin/Mineral Supplements
In response to findings by the State-of-the-Science Conference on Multivitamin/Mineral Supplements and Chronic Disease Prevention, the National Nutritional Foods Association (NNFA) maintains that multivitamins and other mineral supplements taken by more than 100 million Americans daily are a safe, affordable and effective way to maintain a healthy lifestyle.
- NNFA Statement in Response to NIH State-of-the-Science Conference on Multivitamin/Mineral Supplements
In response to findings by the State-of-the-Science Conference on Multivitamin/Mineral Supplements and Chronic Disease Prevention, the National Nutritional Foods Association (NNFA) maintains that multivitamins and other mineral supplements taken by more than 100 million Americans daily are a safe, affordable and effective way to maintain a healthy lifestyle.
- FDA Finalizes Health Claim Associating Consumption of Barley Products with Reduction of Risk of Coronary Heart Disease
The Food and Drug Administration announced that it has finalized a rule that allows foods containing barley to claim that they reduce the risk of coronary heart disease. whole grain barley and dry milled barley products such as flakes, grits, flour, and pearled barley, which provide at least 0.75 grams of soluble fiber per serving, may bear the following claim: ""Soluble fiber from foods such as [name of food], as part of a diet low in saturated fat and cholesterol, may reduce the risk of heart disease. A serving of [name of food] supplies [x] grams of the soluble fiber necessary per day to have this effect."
- FDA Finalizes Health Claim Associating Consumption of Barley Products with Reduction of Risk of Coronary Heart Disease
The Food and Drug Administration announced that it has finalized a rule that allows foods containing barley to claim that they reduce the risk of coronary heart disease. whole grain barley and dry milled barley products such as flakes, grits, flour, and pearled barley, which provide at least 0.75 grams of soluble fiber per serving, may bear the following claim: ""Soluble fiber from foods such as [name of food], as part of a diet low in saturated fat and cholesterol, may reduce the risk of heart disease. A serving of [name of food] supplies [x] grams of the soluble fiber necessary per day to have this effect."
- FDA Finalizes Health Claim Associating Consumption of Barley Products with Reduction of Risk of Coronary Heart Disease
The Food and Drug Administration announced that it has finalized a rule that allows foods containing barley to claim that they reduce the risk of coronary heart disease. whole grain barley and dry milled barley products such as flakes, grits, flour, and pearled barley, which provide at least 0.75 grams of soluble fiber per serving, may bear the following claim: ""Soluble fiber from foods such as [name of food], as part of a diet low in saturated fat and cholesterol, may reduce the risk of heart disease. A serving of [name of food] supplies [x] grams of the soluble fiber necessary per day to have this effect."
- FDA Finalizes Health Claim Associating Consumption of Barley Products with Reduction of Risk of Coronary Heart Disease
The Food and Drug Administration announced that it has finalized a rule that allows foods containing barley to claim that they reduce the risk of coronary heart disease. whole grain barley and dry milled barley products such as flakes, grits, flour, and pearled barley, which provide at least 0.75 grams of soluble fiber per serving, may bear the following claim: ""Soluble fiber from foods such as [name of food], as part of a diet low in saturated fat and cholesterol, may reduce the risk of heart disease. A serving of [name of food] supplies [x] grams of the soluble fiber necessary per day to have this effect."
- FDA Finalizes Health Claim Associating Consumption of Barley Products with Reduction of Risk of Coronary Heart Disease
The Food and Drug Administration announced that it has finalized a rule that allows foods containing barley to claim that they reduce the risk of coronary heart disease. whole grain barley and dry milled barley products such as flakes, grits, flour, and pearled barley, which provide at least 0.75 grams of soluble fiber per serving, may bear the following claim: ""Soluble fiber from foods such as [name of food], as part of a diet low in saturated fat and cholesterol, may reduce the risk of heart disease. A serving of [name of food] supplies [x] grams of the soluble fiber necessary per day to have this effect."
- FDA Finalizes Health Claim Associating Consumption of Barley Products with Reduction of Risk of Coronary Heart Disease
The Food and Drug Administration announced that it has finalized a rule that allows foods containing barley to claim that they reduce the risk of coronary heart disease. whole grain barley and dry milled barley products such as flakes, grits, flour, and pearled barley, which provide at least 0.75 grams of soluble fiber per serving, may bear the following claim: ""Soluble fiber from foods such as [name of food], as part of a diet low in saturated fat and cholesterol, may reduce the risk of heart disease. A serving of [name of food] supplies [x] grams of the soluble fiber necessary per day to have this effect."
- FDA Finalizes Health Claim Associating Consumption of Barley Products with Reduction of Risk of Coronary Heart Disease
The Food and Drug Administration announced that it has finalized a rule that allows foods containing barley to claim that they reduce the risk of coronary heart disease. whole grain barley and dry milled barley products such as flakes, grits, flour, and pearled barley, which provide at least 0.75 grams of soluble fiber per serving, may bear the following claim: ""Soluble fiber from foods such as [name of food], as part of a diet low in saturated fat and cholesterol, may reduce the risk of heart disease. A serving of [name of food] supplies [x] grams of the soluble fiber necessary per day to have this effect."
- FDA Finalizes Health Claim Associating Consumption of Barley Products with Reduction of Risk of Coronary Heart Disease
The Food and Drug Administration announced that it has finalized a rule that allows foods containing barley to claim that they reduce the risk of coronary heart disease. whole grain barley and dry milled barley products such as flakes, grits, flour, and pearled barley, which provide at least 0.75 grams of soluble fiber per serving, may bear the following claim: ""Soluble fiber from foods such as [name of food], as part of a diet low in saturated fat and cholesterol, may reduce the risk of heart disease. A serving of [name of food] supplies [x] grams of the soluble fiber necessary per day to have this effect."
- BioEnvelop Gains Registration with Health Canada for Manufacturing of Natural Health Products
Company has received a license to manufacture under the Natural Health
Products (NHP) certification program of Canada.
- 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
|
FTC Charged They Could Not Back Up Claims for Six Weight-Loss Products for Adults and Kids
Sellers making questionable weight-loss and fat-loss claims to peddle skin gels and diet supplements will pay $3 million to settle Federal Trade Commission charges that their deceptive claims violated federal law. The settlement bars unsubstantiated claims in the future and bars the marketers from misrepresenting studies or endorsements.
According to the FTC’s Complaint, the ads for three skin gels – Tummy Flattening Gel, Cutting Gel, and Dermalin APg – claimed they melted away fat wherever applied, including a user’s thighs, tummy, even a double chin. Ads for Leptoprin and Anorex, two ephedrine pills, claimed they caused weight loss of more than 20 pounds. The advertising for PediaLean fiber pills for overweight children claimed the pills caused substantial weight loss. The FTC alleged the marketers lacked a reasonable basis to back up these claims. In addition, the FTC alleged the ads falsely claimed that clinical testing proved those claims for four of the challenged products and misrepresented their spokesperson as a medical doctor.
Ads for the products ran on television, in magazines, and in tabloids. The products were also marketed on the Internet. Leptoprin was heavily advertised through short-form television infomercials. Ads for the skin gels ran in Cosmopolitan, Muscle and Fitness, and other magazines. PediaLean was advertised in tabloids and magazines such as The Enquirer and Redbook.
Under the FTC’s final order, the primary company, Basic Research, will pay $3 million on behalf of all six companies and three individuals charged in this case: Basic Research, LLC, A.G. Waterhouse, LLC, Klein Becker USA, LLC, NutraSport, LLC, Sovage Dermalogic Laboratories, LLC, BAN LLC, Dennis Gay, Daniel B. Mowrey (also doing business as American Phytotherapy Research Laboratory) and Mitchell K. Friedlander.
The FTC’s final order prohibits the marketers from making unsubstantiated claims that Dermalin-APg, Cutting Gel, Tummy Flattening Gel, Anorex, Leptoprin, PediaLean, or any substantially similar product causes weight loss or fat loss and misrepresenting the effects of a product through the use of product names or endorsements. When they make weight-loss or fat-loss claims for any products, they must rely on competent and reliable scientific evidence. The marketers must also have substantiation to support representations that any food, drug, or dietary supplement has an effect on any disease, on the structure or function of the human body, or other health or weight-loss benefits. They cannot misrepresent any test, study, or research, or the profession, expertise, training, education, experience, or qualifications of any endorser.
The Commission vote to accept the consent agreement, subject to public comment, was 5-0. The FTC will publish an announcement regarding the agreement in the Federal Register. The agreement will be subject to public comment for 30 days, beginning today and ending Monday, June 12, 2006. Comments should be addressed to the FTC, Office of the Secretary, Room H-135, 600 Pennsylvania Avenue, N.W., Washington, DC 20580. The FTC requests that any comment filed in paper form be sent by courier or overnight service, if possible, because U.S. postal mail in the Washington area and at the Commission is subject to delay due to heightened security precautions.
NOTE: A consent agreement is for settlement purposes only and does not constitute an admission of a law violation. When the Commission issues a consent order on a final basis, it carries the force of law with respect to future actions. Each violation of such an order may result in a civil penalty of $11,000.
Copies of the complaint, proposed consent agreement, and an analysis of the agreement to aid in public comment 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 thousands of civil and criminal law enforcement agencies in the U.S. and abroad. |