Ashwagandha Extract
Withania somnifera
Withanolides 2.5% – 10%SV Botanica provides certified, wholesale herbal extract supply designed specifically for supplement brands, contract development and manufacturing organisations (CDMOs), and private-label formulators globally. Sourced and processed in India under strict cGMP environments, our botanical portfolio covers over 60 active extracts engineered to meet the stringent physical, chemical, and microbiological thresholds required for solid dose encapsulation, tableting, effervescents, and liquid formulations.
From clean-label demands to high-speed encapsulation, our active botanical extracts solve common production and compliance bottlenecks before raw materials arrive at your plant.
Guaranteed active phytochemical percentages (withanolides, curcuminoids, bacosides, silymarin) verified by HPLC, UV, or titration methods defined clearly on each CoA.
Complete documentation packages supplied as standard: complete batch CoA, Safety Data Sheets (SDS), technical specifications, allergen matrices, and non-GMO statements.
Strict particle-size control (40 to 80 mesh) and consistent bulk density ensure superior flowability, minimal die-wall friction, and uniform blend distribution.
Comprehensive third-party validation covering pesticide multiresidues (EU MRLs), ethylene oxide (ETO), irradiation screens, and ICP-MS elemental impurities.
Our most widely requested botanical extracts for dietary supplements, dietary foods, and functional nutrition brands, backed by batch-level verification.
Withania somnifera
Withanolides 2.5% – 10%Curcuma longa
Curcuminoids ≥ 95.0%Boswellia serrata
Boswellic Acids 35% – 75%Bacopa monnieri
Bacosides 20% – 50%Berberis aristata
Berberine HCl 97% – 98%Hericium erinaceus
Beta-Glucans 30% – 40%Silybum marianum
Silymarin Up to 80%Rhodiola rosea
Rosavins 3% · Salidroside 1%We do not treat documentation as an administrative afterthought. Every consignment is treated as an audited regulatory deliverable designed for seamless clearance through customs and QA quarantine.
Identity verification through TLC/HPTLC fingerprinting and quantitative assay analysis using calibrated HPLC instrumentation aligned to pharmacopoeial monographs.
Reference: USP / EP / BP MonographsRigorous ICP-MS quantification for lead, arsenic, cadmium, and mercury, paired with complete microbiological screens (aerobic plate count, yeast & mold, Salmonella, E. coli).
Ref: Regulation (EU) 2023/915 · USP <2232>Every commercial lot arrives with a signed CoA, Technical Data Sheet, 16-section SDS, allergen statement, residual solvent screen (USP <467>), and non-irradiation certificate.
FSMA / FSVP Ready DocumentationA rigorous supply protocol engineered around QA approval and specification alignment, ensuring complete transparency prior to bulk manufacturing.
Submit your target monograph, active marker percentage, physical density, mesh requirement, and annual forecast.
Day 0Our quality assurance desk provides a matching specification sheet, representative CoA, and firm freight pricing.
Within 24 HoursWe supply bench-scale validation samples with lot CoAs for laboratory verification and pilot formulation testing.
QC Sign-OffFinal testing, release documentation, vacuum-sealed barrier packaging, and international freight dispatch.
On-Schedule DeliveryAnalytical methodologies, international compliance protocols, and technical evaluations curated by our scientific regulatory desk.
Comprehensive breakdown of official controls, ethylene oxide (ETO) testing requirements, and pesticide multiresidue monitoring under Regulation (EU) 2019/1793.
Technical evaluation of HPLC versus gravimetric testing, solvent selection risks, and plant-part authenticity in commercial Withania somnifera extracts.
Why UV-Vis spectrophotometry overstates curcuminoid potency and how HPLC testing ensures accurate dosage compliance for brand integrity.
Critical specifications for commercial Berberis aristata extracts, heavy metal controls, and addressing solvent screening parameters.
Direct answers concerning quality assurance, batch verification, and commercial shipping terms for dietary supplement brands.
We supply standardised active extracts including Ashwagandha, Turmeric Curcumin 95%, Boswellia Serrata, Berberine HCl, Brahmi (Bacopa monnieri), Milk Thistle, Lion's Mane, Rhodiola, and over 60 other botanical actives tailored for solid doses, capsules, and drink mixes.
All active phytochemical compounds (such as withanolides, curcuminoids, and boswellic acids) are quantified using validated HPLC, UV, or titration methods. The exact chromatographic assay method is documented explicitly on every lot Certificate of Analysis.
Every shipment comes complete with a Batch Certificate of Analysis (CoA), Technical Data Sheet (TDS), Safety Data Sheet (SDS/MSDS), ICP-MS heavy metals report, microbial profile, allergen statement, non-GMO declaration, and destination-specific phytosanitary certificates.
Standard MOQs typically start at 25 kg per ingredient in sealed, food-grade fibre drums. We also facilitate custom pilot-batch volumes and multi-metric-ton container loads for large contract manufacturers.
Yes. We dispatch pre-shipment samples accompanied by lot-specific Certificates of Analysis so R&D and QC departments can perform complete bench testing, flowability evaluations, and analytical verifications before release.
Connect with our technical exports desk for immediate assistance with active standardisations, analytical validation dossiers, and wholesale quotation terms.
Fast-track your procurement evaluation. Our regulatory and logistics teams provide technical data sheets, full batch CoAs, and pricing within one business day.