XYMOGEN
Violation History
1 incident
Fda Warning
The warning letter cited violations of current Good Manufacturing Practice (cGMP) regulations for dietary supplements, including failure to establish product specifications for the identity, purity, strength, and composition of the finished dietary supplement, and failure to conduct at least one appropriate test or examination to verify the identity of a dietary ingredient. The letter also noted that several products were considered new drugs because they were not generally recognized as safe and effective for their intended use.2011-12-13Source
SAM-e, 30 Acid-Resistant Vegetarian Capsules
Product 62
Brand 96
GastrAcid, 180 Vegetarian Capsules
Product 62
Brand 96
DHEA Micronized, 10 mg, 60 Tablets
Product 62
Brand 96
Red Yeast Rice, 60 Vegetarian Capsules
Product 62
Brand 96
SynovX Tendon & Ligament, 60 Vegetable Capsules
Product 62
Brand 96
ProteoXyme, 100 Acid-Resistant Vegetarian Capsules
Product 61
Brand 96
Leptin Manager, 30 Vegetarian Capsules
Product 59
Brand 96
OSAplex, 60 Packets
Product 58
Brand 96
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Disclaimer: GoodSupp provides independent supplement quality analysis for informational purposes only. Scores are generated algorithmically based on ingredient profiles, brand certifications, and public records. This is not medical advice. Always consult a healthcare professional before starting any supplement regimen. Product data is sourced from manufacturer labels and public databases. GoodSupp is not affiliated with any supplement brand.