RegulyzeAkarkar
Akarkar is a botanical permitted for use in nutraceuticals and health supplements under India's FSSAI framework, with a permitted limit of 100-250 mg (as powder). Regulyze tracks its regulatory status, limits and label requirements across regulatory frameworks.
Regulatory status
| Framework | Status | Limit | Source | Last reviewed |
|---|---|---|---|---|
| India — FSSAI | Permitted | 100-250 mg (as powder) | FSS (Health Supplements, Nutraceuticals…) Regulations 2022 | 2026-06-20 |
Coverage for the USA (FDA), EU (EFSA), UK, GCC and ASEAN is being added — this page updates automatically as frameworks are assessed.
About Akarkar
Akarkar is tracked in the Regulyze Ingredient Intelligence database as a botanical. The regulatory details on this page are generated from Regulyze's structured regulatory dataset and are reviewed against the cited source.
Frequently asked questions
Is Akarkar permitted in nutraceuticals under FSSAI (India)?
Akarkar is currently permitted for use in health supplements and nutraceuticals under India's FSSAI framework, per FSS (Health Supplements, Nutraceuticals…) Regulations 2022. Always verify against the current official regulation for your product and market.
What is the permitted dosage of Akarkar?
The permitted level recorded for Akarkar is 100-250 mg (as powder). Limits can vary by product type and market — confirm against the current regulation.
What product category does Akarkar belong to?
Akarkar is classified under: Botanicals.
Source: FSS (Health Supplements, Nutraceuticals…) Regulations 2022 · Last reviewed: 2026-06-20 · Data version: db-2026-06-20. Indicative only — verify against the current official regulation before use.