RegulyzeBibhitaki
Terminalia bellirica · Fruit
Bibhitaki (Terminalia bellirica) is a botanical permitted for use in nutraceuticals and health supplements under India's FSSAI framework, with a permitted limit of 3-5 g; Extract: 0.5-1 g. Regulyze tracks its regulatory status, limits and label requirements across regulatory frameworks.
Regulatory status
| Framework | Status | Limit | Source | Last reviewed |
|---|---|---|---|---|
| India — FSSAI | Permitted | 3-5 g; Extract: 0.5-1 g | 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 Bibhitaki
Bibhitaki is tracked in the Regulyze Ingredient Intelligence database as a botanical (Terminalia bellirica). It is listed in India's FSSAI schedules under the regulatory name Bibitaki / Bahera. 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 Bibhitaki permitted in nutraceuticals under FSSAI (India)?
Bibhitaki (Terminalia bellirica) (listed in the regulation as “Bibitaki / Bahera”) 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 Bibhitaki?
The permitted level recorded for Bibhitaki is 3-5 g; Extract: 0.5-1 g. Limits can vary by product type and market — confirm against the current regulation.
What product category does Bibhitaki belong to?
Bibhitaki is classified under: Botanicals.
What is the botanical (scientific) name of Bibhitaki?
Bibhitaki corresponds to Terminalia bellirica, with the fruit used in nutraceutical preparations.
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.