Speciality ingredient · Available under NDA
Arvena Sciences has developed a proprietary preparation of Glycyrrhiza glabra (Mulethi / licorice root), available as a specialty active ingredient to supplement manufacturers under a signed NDA. Because it comes from a regulatory consultancy, not just an ingredient supplier, you get the compliance groundwork alongside the ingredient itself.
Available to supplement manufacturers · Under NDA
Arvena Sciences has developed a proprietary active ingredient based on Glycyrrhiza glabra (Mulethi) — processed through a unique, fully proprietary preparation methodology developed and refined over 12 years of systematic observation.
Glycyrrhiza glabra has a well-documented traditional and scientific track record as an immunity-supporting botanical, recognised across Ayurvedic, Traditional Chinese, and European herbal medicine systems. The Arvena Sciences preparation takes this established botanical into a new dimension through its proprietary process.
The preparation is used at trace ratios of 1:200 to 1:500 as an active ingredient in finished supplement formulations. At these ratios it is exceptionally cost-effective, adds no perceptible taste or texture, and carries no known side effects even at higher concentrations. It is fully compatible with capsule, sachet, tablet, and liquid supplement formats.
The preparation methodology, process details, and ratio specifications are proprietary and not publicly disclosed. Details are shared verbally with serious manufacturers under a signed NDA. We do not make claims about outcomes — we invite manufacturers to experience results through a supervised sample trial.
For serious manufacturers only
We offer a paid sample programme for manufacturers who want to validate the ingredient in their own formulation before any licensing commitment:
Methodology, preparation process, and ratio specifications are proprietary. Per our NDA policy, details cannot be disclosed publicly.
Enquire under NDAA standardized, quality-controlled Mulethi preparation, with full technical and safety documentation shared under NDA.
Because we're a regulatory consultancy first, we scope the FSSAI and target-export-market approval pathway for your specific formulation alongside the ingredient supply conversation — not as a separate, later engagement.
Dosage, combination, and stability guidance drawn from the same formulation research that produced the ingredient in the first place.
Tell us about your product and we'll take the conversation from there, under NDA.
Enquire under NDA