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Preview — digitized from the official gazettes and checked automatically against the page each row cites. 831 of 832 FSSAI ingredient rows have been signed off by a person — some in bulk from the machine extraction rather than read page by page, so confirm against the gazette before you rely on a result. The 732 CDSCO rows behind a drug classification carry no human review at all.
Regulation bulletinLegal Metrology (Packaged Commodities) Rules — amendments changed since the last sweep — review for schedule or limit changes. (under review — not yet applied)23 Sept 2026

Government sources last swept 17h ago. 2 of 7 sources could not be fetched on the last sweep (FSSAI notifications (gazette, draft, ordinary), FSSAI nutraceutical regulation amendments), so changes to them would not have been detected. Verify against the gazette before relying on this. Detected changes are triaged by a human before any data moves.

Dolly Intelligence

State licensing authorities

FSSAI permitted-ingredient schedules are central and uniform across India — states do not maintain different permitted lists. What varies by state is licensing, enforcement posture, and any No Objection Certificate for export-oriented manufacture. These are the offices to contact.

36 of 36 states/UTs · source: FSSAI Commissioners of Food Safety directory · last verified 2026-08-05

Dolly Intelligence highlights the route and the office to approach. The authority decides — nothing here anticipates their decision or substitutes for their determination.