Standardised Herbal Extracts Exporter
70+ pharmacopoeial botanical extracts manufactured in GMP-certified facilities. Complete lot traceability, HPLC-validated markers, and EU/US regulatory dossier support.
Bulk Botanical Extracts Catalogue
Browse our core inventory of 70 standardised extracts. Each item is manufactured under stringent in-process controls, assayed via validated chromatographic methods, and supplied in drum quantities for global export.
No botanical extracts match your search
We frequently custom-extract botanical species and standardisation markers not listed in the standard inventory.
Send an InquiryExport Compliance & Analytical Rigour
International regulatory authorities demand uncompromised data integrity. Every botanical extract manufactured for export is subjected to rigorous multi-tiered verification before batch release.
Chromatographic Identity
Active markers validated via High-Performance Liquid Chromatography (HPLC), Ultra-Violet Spectrophotometry (UV-Vis), or Titration as defined in USP/BP/Ph. Eur. pharmacopoeias.
Pesticide MRL Compliance
Extensive multi-residue panels performed by accredited third-party laboratories to ensure complete conformity with EU Regulation (EC) No 396/2005 and US FDA food residue tolerance levels.
Heavy Metals by ICP-MS
Routine screening for Lead (Pb), Cadmium (Cd), Arsenic (As), and Mercury (Hg) compliant with EU 2023/915 and USP <232>/<233> elemental impurity thresholds.
ETO & Pathogen Safeguards
100% verified Ethylene Oxide free (ETO < 0.05 mg/kg for 2-chloroethanol) and fully tested for Total Viable Aerobic Count, Yeast & Mould, Salmonella, and E. coli.
Dietary Supplements & VMS
Optimized for hard-shell encapsulation, two-piece capsules, tableting direct compression, and active botanical gummy formulations with consistent tapped density.
Functional Foods & RTD Beverages
Micro-pulverized water-soluble and dispersible botanical extracts developed for nutritional drink powders, functional wellness shots, and fortified RTD liquids.
Dermaceuticals & Personal Care
Purified active fractions engineered for topically stable skincare serums, anti-ageing creams, clarifying formulations, and bioactive scalp treatments.
Frequently Asked Questions
Essential regulatory, technical, and logistics information for sourcing managers, analytical chemists, and corporate QA teams evaluating our Indian herbal extract supply chain.
Our standard export minimum order quantity is 25 kg per individual botanical extract, supplied in industrial fibre drums with inner poly-liners. For formulation trials, R&D piloting, or multi-item blended shipments, pilot evaluation volumes of 5 kg to 10 kg can be accommodated upon request.
Every export lot is dispatched with a full regulatory packet including a batch Certificate of Analysis (CoA) specifying the exact assay methodology, Safety Data Sheet (SDS) compliant with GHS, Technical Data Sheet (TDS), Phytosanitary Certificate issued by Indian Plant Quarantine, and Certificate of Origin. Comprehensive third-party pesticide multi-residue screens, ICP-MS heavy metal reports, and ETO-free certifications are supplied as standard for European and North American buyers.
Yes. Production takes place in state-of-the-art facilities compliant with WHO-GMP and ISO 22000 management standards. For the European Union, testing conforms to Regulation (EC) No 396/2005 (MRLs) and Regulation (EU) 2023/915 for heavy metals and mycotoxins. For the United States, our QA package directly supports buyer compliance under 21 CFR Part 111 (Dietary Supplement cGMP) and the Foreign Supplier Verification Program (FSVP).
Yes. In addition to our standard catalogue specifications, our extraction units can formulate bespoke marker concentrations, carrier-free or organic maltodextrin carrier additions, specific granulations (e.g., 40 to 120 mesh), and cold-water-soluble formulations tailored to solid dose, ready-to-mix beverage, or cosmetic systems.
Yes. We provide representative 50 g to 100 g lot evaluation samples together with complete analytical CoAs. This allows your QC, R&D, and analytical teams to verify physical characteristics, chromatographic fingerprinting, and purity before commercial production lots are dispatched.