We know that the human growth hormone is a hormone that is secreted by the pituitary gland, but when an excess, if found present in the body (through supplementation), the body will naturally start to stimulate the liver and other tissue to secrete another hormone called IGF-1. This dietary supplement processes carbohydrates in your body as they are put to use and increases the production of AMPK for weight loss. On the same line, you must list the total weight of all “other dietary ingredients” contained in the blend. Indented underneath the name of the blend, you must list the “other dietary ingredients” in the blend, either in a column or linear fashion, in descending order of predominance by weight. You may list constituents of a dietary ingredient indented under the dietary ingredient and followed by their quantitative amounts by weight per serving.
You must list liquid extracts using the volume or weight of the total extract and the condition of the starting material before extraction when it was fresh. For dietary ingredients extracted from which the solvent has been removed, you must list the weights of the dried extracts. The solvent must be identified in either the nutrition label or ingredient list. You may include information on the concentration of the dietary ingredient and the solvent used. The regulation states that the term “high potency” may be used in a claim on the label or in labeling to describe individual vitamins or minerals that are present at 100 percent or more of the Reference Daily Intakes (RDI) per reference amount customarily consumed (21 CFR 101.54(f)(1)(i)). This means a supplement may be labeled as “high potency” for each nutrient(s) present at 100% of the RDI per serving.
The Federal Trade Commission (“FTC”) has sua non mama overlapping jurisdiction with the federal Food and Drug Administration (“FDA”) and focuses more on whether advertising is truthful, or false and misleading. Among other requirements, food must be labeled as “low calorie” or “reduced calorie” or bear a relative claim of special dietary usefulness. You must identify proprietary blends using the term “Proprietary Blend” or an appropriately descriptive term or fanciful name. FDA will permit the use of a qualified health claim provided that 1) FDA has issued a letter stating the conditions under which we will consider exercising enforcement discretion for the specific health claim, 2) the qualified claim is accompanied by an agency-approved disclaimer, and 3) the claim meets all the general requirements for health claims in 21 CFR 101.14, except for the requirement that the evidence for the claim meets the validity standard for authorizing a claim, and the requirement that the claim is made by an authorizing regulation.