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There is no single product category for our health food products in the USA. Most health food products can be classified as Dietary Supplement or general food with functional claims, and all of them fall within the scope of food regulation. Next, let's take a look at the scope of a Dietary Supplement in the United States and the regulatory authorities. Here are some answers.

Here is the content list:

l The scope of Dietary Supplement in the USA.

l Regulatory authority for Dietary Supplement in the United States.

The scope of Dietary Supplement in the USA.

A Dietary Supplement is a product (not tobacco) intended to supplement the diet and may contain one or more of the following dietary ingredients: vitamins, minerals, herbs (herbal) or other plants, amino acids, and dietary ingredients to increase the total daily intake, or a concentrate, metabolite, extract or combination of these ingredients. It may not be consumed in the form of tablets, capsules, powders, soft gels, or oral liquids; it may not be consumed as a conventional food or as the sole component of a meal diet. DSHEA also allows the use of pharmaceutical ingredients, such as approved or licensed new drugs, antibiotics, biologics, etc., provided that they have been marketed as Immunity increases or food before the relevant approval, certification, or licensing; however, if they have not been marketed as a Dietary Supplement or food before the relevant approval or certification, they may not be used as a Dietary Supplement. However, if the substance has not been marketed as a Dietary Supplement or food before the relevant approval or certification, it may not be used in Dietary Supplement.

Regulatory authority for Dietary Supplement in the United States.

The US Food and Drug Administration (FDA), one of the federal executive agencies of the Department of Health and Human Services (HHS), is the regulatory authority for Dietary Supplement, which is different from "conventional" foods and drugs, primarily under DSHEA, which was established in 1994. Dietary Supplements and Dietary Ingredients Manufacturers and distributors of dietary supplements and dietary ingredients are responsible for assessing the safety and labeling of their products before marketing to ensure that they meet all the requirements of DSHEA and the relevant FDA regulations. The Centre for Food Safety and Applied Nutrition (CFSAN) is responsible for the safety and labeling of the Hard capsules. The National Institutes of Health (NIH), one of the HHS divisions, focuses on scientific research and the NIH Office of Dietary Supplement (ODS) coordinates the overall management of the Dietary Supplement. The common goal of NIH and FDA is to promote public health by facilitating the translation of basic and clinical research into medical products and treatments. These agencies complement each other in their roles and functions: NIH supports and conducts biomedical and behavioral research, and FDA ensures the safety and efficacy of medical and other products. In addition, the Committee on Dietary Supplement Labelling (CDSL) examines the regulatory and Dietary Supplement claims on labels and provides recommendations on how best to provide consumers with information that is truthful, scientifically valid, and not misleading. The Commission is composed of seven members appointed by the President. The members of the committee should have expertise and experience in the manufacture, regulation, distribution, and use of Dietary Supplement. At least three of the members should have scientific training and experience to assess the health benefits of Dietary Supplement use, and one of the members should have experience in pharmacology, medical botany, traditional herbal medicine, or other science-related fields. Committee members and staff should be free from bias on Dietary Supplement issues.

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Omega-3 fatty acids are found in foods, such as fish and flaxseed, and in dietary supplements, such as fish oil.

The three main omega-3 fatty acids are alpha-linolenic acid (ALA), eicosapentaenoic acid (EPA), and docosahexaenoic acid (DHA). ALA is found mainly in plant oils such as flaxseed, soybean, and canola oils. DHA and EPA are found in fish and other seafood.

ALA is an essential fatty acid, meaning that your body can’t make it, so you must get  it from the foods and beverages you consume. Your body can convert some ALA into EPA and then to DHA, but only in very small amounts. Therefore, getting EPA and  DHA from foods (and dietary supplements if you take them) is the only practical way to increase levels of these omega-3 fatty acids in your body.

Omega-3s are important components ofthe membranes that surround each cell in    your body. DHA levels are especially high in retina (eye), brain, and sperm cells.Omega-3s also provide calories to give your body energy and have many functions in your heart, blood vessels, lungs, immune system, and endocrine system (the network of hormone-producing glands).

How much omega-3s do I need?

Experts have not established recommended amounts for omega-3 fatty acids, except   for ALA. Average daily recommended amounts for ALA are listed below in grams (g). The amount you need depends on your age and sex.

Fish oil supplements

Sulfur is essential, but for humans, it is not recommended for intake. Instead, recommended intakes have been established for the sulfur-containing amino acids methionine and cysteine. There are Dietary Supplements that provide sulfur, such as taurine. Next, let's take a look at the types of Dietary Supplements available. Here are some answers.

Here is the content list:

l Minerals

l Protein and amino acids

Minerals

Although, in general, Dietary Supplements are not allowed to be labeled and marketed with claims of disease prevention or treatment, the US Food and Drug Administration (FDA) has conducted a scientific review of certain foods and Dietary Supplements. They concluded that there is a significant scientific consensus and specifically published permissible health words. An initial ruling allowing health claims for calcium Dietary Supplements and osteoporosis was later amended to include calcium supplements with or without vitamin D, effective January 1, 2010. Examples of the permitted wording are shown below. To meet the health requirement for calcium, Health care must contain at least 20% of the reference dietary intake, which for calcium means at least 260 mg/serving.

In the same year, the European Food Safety Authority approved Dietary Supplement's health claims for calcium and vitamin D, which can reduce the risk of osteoporotic fractures by reducing bone loss. The US FDA has also approved Qualified Health Claims (QHC) for calcium, selenium, and chromium picolinate for various health conditions, which have scientific evidence but do not meet the more stringent "significant scientific agreement" criteria required for authorized health claims. If Hard capsules choose to make such a claim, the FDA specifies the exact wording of the QHC to be used in labeling and marketing materials. The wording could be cumbersome: "One study suggests that selenium intake may reduce the risk of bladder cancer in women. However, another smaller study showed that the risk was not reduced. Based on these studies, the FDA concludes whether selenium supplements may reduce the risk of bladder cancer in women."

Protein and amino acids

Whey protein is a popular ingredient, but products may also contain casein, soy, pea, and rice proteins. The same protein ingredients as those commercially available in Immune Supports can be incorporated into meal replacements and medical foods, but they are administered and labeled differently from supplements. In the US, "meal replacement" products are food products and are labeled accordingly. These usually contain protein, carbohydrates, fats, vitamins, and minerals. There may be claims such as "good source of protein", "low fat" or "lactose-free". It also designed to be a nutritionally complete medical food that is used under the care of a doctor or other licensed healthcare professional.

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Scientists are studying omega-3s to understand how they affect health. People who eat fish and other seafood have a lower risk of several chronic diseases. But it is not clear  whether these health benefits come from simply eating these foods or from the omega-3s in these foods. Here are some examples ofwhat the research has shown.

Cardiovascular disease

Many studies show that eating fatty fish and other types of  seafood as part of a healthy eating pattern helps keep your heart healthy and helps protect you from some heart problems. Getting more EPA and DHA from foods or dietary supplements lowers triglyceride levels, for example.

The American Heart Association (AHA) recommends eating   one to two servings of seafood per week to reduce your risk of some heart problems, especially if you consume the seafood  in place of less healthy foods. For people with heart disease,the AHA recommends consuming about 1 g per day EPA plus DHA, preferably from oily fish, but supplements are an option under the guidance ofa healthcare provider. The AHA does not recommend omega-3 supplements for people who do not have a high risk of cardiovascular disease.

Health food is a supplement based on vitamins, minerals, and extracts with a relatively clear structure-activity relationship, which is taken orally to supplement essential nutrients and bioactive substances to improve health and reduce the risk of disease. The following Dietary Supplement manufacturers will introduce you to the characteristics and requirements of Dietary Supplements. Here are some answers.

Here is the content list:

l What are the characteristics of Dietary Supplements?

l What requirements must a Dietary Supplement meet?

What are the characteristics of Dietary Supplements?

What are the ingredients of Dietary Supplements?

The raw materials used in Dietary Supplement are mainly taken from natural species, but there are also safe and reliable substances produced through chemical or biological technology, such as plant and animal extracts, vitamins, minerals, amino acids, etc. Generally speaking, the physical and chemical properties of the functional ingredients are relatively stable, the chemical structure is relatively clear, the mechanism of action has been scientifically proven to a certain extent, and the safety, functionality, and quality control meet the regulatory standards.

What is the form of Dietary Supplement?

Dietary Supplement is mainly available in the form of pharmaceutical-like products in the following dosage forms: hard capsules, soft capsules, tablets, oral liquids, granules, powders, etc. The packaging forms are pre-packaged in bottles, drums (boxes), bags, and aluminum blister packs.

Health standards for Dietary Supplement.

Immunity increases with the status of general food can follow the requirements of the "Nutritional Labelling Regulation for Food" issued by the Ministry of Health in 2008 and label the product with nutrition or nutrient function claims. Health food products approved by the health administration can only claim the specific health functions approved, and the publication of advertisements needs to be approved by the State Drug Administration. Dietary Supplement, on the other hand, can only claim to supplement (specifically) nutrients.

What requirements must a Dietary Supplement meet?

Firstly, Dietary Supplement containing more than three (inclusive) vitamins and minerals can only be described as a complex or multiple Dietary Supplement. The label and instructions should indicate each content, recommended intake, method of storage and precautions, etc. Thirdly, Dietary Supplements should consist of one or more vitamins or minerals in the form of tablets, capsules, tablets, or oral liquid; the daily consumption of tablets should not exceed 20 grams and the daily consumption of oral liquid should not exceed 30 ml. Fourthly, Dietary Supplements must obtain a health food approval certificate before they can be manufactured and sold. Fifthly, the excipients added to Dietary Supplements should be mainly to enhance the product's process performance or improve the taste of the product. Sixth, the raw materials and excipients in Skin care should provide their sources and quality standards; chemically synthesized Dietary Supplement raw materials should be "Hygienic Standards for the Use of Food Additives", the relevant circulars of the Ministry of Health or the Pharmacopoeia of the types of Dietary Supplement raw materials allowed to be used and comply with the corresponding provisions, otherwise, Otherwise, it should be evaluated for safety and toxicology concerning the requirements for new food resources and provide scientific proof of safe human intake.

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