MEDIOCON INC offers Kiwi Seed Extract, a botanical extract obtained from the seeds of kiwi fruit, Actinidia chinensis Planch. Kiwi seed extract contains naturally occurring polyphenolic constituents, including quercitrin, and is available in food and nutraceutical ingredient formats. A published food-grade product specification describes kiwi seed extract as a powder obtained by aqueous-ethanol extraction of Actinidia chinensis seeds.
A representative food-grade specification identifies polyphenols at a minimum of 2.0% and quercitrin at a minimum of 5.0 mg/100 g by HPLC. The same specification describes the material as a yellow powder with a slight characteristic odour. These values are representative of the referenced commercial specification and should be confirmed against the applicable batch CoA for the material supplied by MEDIOCON INC.
The commonly listed CAS number for Actinidia chinensis Seed Extract is 92456-63-8.
FSSAI records list Kiwi seed extract under application 14/Std/PA/FSSAI/2018 & 22.06.2018, with M/s Yasham Speciality Ingredients Pvt. Ltd., Andheri (West), Mumbai-400053 as the applicant. The current FSSAI status published as of 3 June 2026 lists this application under Rejected applications.
MEDIOCON INC supplies Kiwi Seed Extract according to applicable product specifications, quality requirements and available technical documentation.
| Parameter | Specification |
|---|---|
| Appearance | Yellow powder with light characteristic odour. |
| Loss on Drying | NMT 10.0%. |
| Heavy Metals | NMT 10 ppm. |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Kiwi Seed Extract Manufacturer & Supplier in India | MEDIOCON INC (CAS 92456-63-8) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Kiwi Seed Extract Manufacturer & Supplier in India | MEDIOCON INC is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing before release with a Certificate of Analysis.
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