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Starting at a higher dose dramatically increases the risk and severity of gastrointestinal side effects
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Batch: GF-AOD10-B241 Key analytical results include: Assay Content: 11.48 mg Identification Retention Time: 0.986 Identification Spectrum: 995 Purity: 99.7 percent Bacterial Endotoxins: below 0.001 EU per mg Total Aerobic Microbial Count: not detected Total Yeast and Mold Count: not detected Independent heavy metal screening confirmed no detectable levels of arsenic, cadmium, cobalt, lead, nickel, mercury or vanadium
In kosmetischen Formulierungen wird der Wirkstoff deshalb hufig eingesetzt, wenn die Haut nach Belastung untersttzt und beruhigt werden soll
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