Verified Company Information
- Legal / Trade Name: JK AGRO INPUTS LLP
- Office: 262, Pragati Park Colony, Sanwar Road, Magar Kheda, Indore, Madhya Pradesh 453111
- Manufacturing Unit: A-5, S.R. Compound, Lasudiya Mori, Dewas Naka, Indore, Madhya Pradesh 453771
Technical vs Company Authorisation
The FCO technical/formulation and the company’s business/manufacturing authorisations are different regulatory layers. The website does not present them as the same thing.
Current Technical Portfolio
- Advance Humic Pro — Humic Acid 19.6% (Liquid)
- Fasal Booster — Protein Hydrolysate 16.9% (Plant Source) (Liquid)
- Amino-25 — Protein Hydrolysates 25% (Plant Source) (Liquid)
- Power Plus 98 — Humic Acid 51% (Granular)
What Is Publicly Verifiable
- Legal company identity
- Product → technical mapping
- Current FCO technical references and specifications
- Official technical/Gazette references
- Existing pack barcode as a secondary verification check
- Last Reviewed / update history
Public Compliance Rule
Licence/permission numbers or documents are not published on the public website as marketing badges. Manufacturing copy states confirmed in-house manufacturing and quality-control capability without turning permissions into promotional claims.
How the Indian Biostimulant Framework Works
India brought biostimulants into the Fertiliser Control Order framework through S.O. 882(E) dated 23 February 2021. For a practical buyer, the important point is that the framework has continued to evolve: Schedule VI entries, specifications and procedural requirements must be read with the latest applicable amendments.
- Schedule VI is the regulatory reference for notified biostimulant identity/specification. Current entries can include active ingredient or tracer molecule/chemical composition, crop/use and analytical/specification details.
- Since the 8 May 2024 amendment, Form G is specifically the application route for inclusion of a NEW biostimulant in Schedule VI, with prescribed chemistry, bio-efficacy, safety/other data as applicable.
- The 2024 amendment also recognised tracer-molecule based specifications and provided toxicology-data exemptions for specified categories including protein hydrolysates, specified seaweeds, amino acids, vitamins, Humic Acid and Fulvic Acid, subject to the prescribed safe-use affidavit.
- The old G3 provisional transition should not be treated as current approval: the Government stated that provisional registrations became invalid from 17 June 2025.
- Schedule VI remains a live regulatory schedule. Later amendments continued in 2026, so current Gazette verification is safer than relying on an old list or a fixed total-product count.
Form G for a New Technical Is Not the Same as Day-to-Day Product Verification
For website and procurement purposes, separate two questions. First: is a technical/formulation currently notified under the applicable FCO framework? Second: is the product in front of you being manufactured, supplied and labelled through the applicable authorised route? Form G concerns inclusion of a new biostimulant in Schedule VI; dealer/buyer verification concerns the current product, source, label, batch and applicable authorisation.