Evidence-informed actives & dosages; excipient strategy; allergen constraints for our custom formulas and nutraceutical solutions. Formats include capsules and powders (others assessed case-by-case). We also offer flavor systems & sweeteners tailored for powders in our private label products. Our label design & printing are aligned with the final formula and claims, ensuring a compliance review for the panel & copy that is FDA/FTC-aligned.
MOQ: typically ≥ 2000; may be higher for certain custom formulas or flavors in our private label products.
Timing: add ~1–3 weeks for R&D/pilot on top of the production timeline for our nutraceutical solutions.
Docs: Spec Sheet + QA Release + QC Summary; COA under NDA (redacted/view-only) or third-party retest.




Quality statement: Manufactured in US GMP-certified, FDA-registered & inspected facilities. Standard documentation includes Batch QC Summary, QA Release Letter, and Finished Product Specifications. COA access under NDA (redacted) or third-party retest available upon request.
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