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The FDA's GRAS determination confirms safety for oral consumption as a food ingredient

FDA's evaluation concluded that the criteria weighed against placement on the list, citing inadequate physicochemical characterization, immunogenicity concerns from impurities and aggregates, lack of clinical effectiveness data for any approved use, and absence of published human exposure data for the proposed subcutaneous and topical routes

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The volume of the injection is usually 1 ml, which corresponds to the standard concentration of 1,000 mcg/ml

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This is particularly beneficial for individuals who suffer from gastrointestinal issues that cause them to have difficulty absorbing food nutrients