Custom Formulas
When a stock base isn’t enough, our R&D team designs to your targets—actives, delivery form, sensory, and cost—then delivers a print-ready label.
Scope
Evidence-informed actives & dosages; excipient strategy; allergen constraints.
Formats: capsules, powders (others case-by-case)
Flavor systems & sweeteners (for powders)
Label design & printing aligned to the final formula and claims
Compliance review for panel & copy (FDA/FTC-aligned)
Operational
MOQ: typically ≥ 2000; may be higher for certain formats/flavors.
Timing: add ~1–3 weeks for R&D/pilot on top of production timeline.
Docs: Spec Sheet + QA Release + QC Summary; COA under NDA (redacted/view-only) or third-party retest.
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Tell us about your project
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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