RegulyzeBabbul
Babbul is a botanical permitted for use in nutraceuticals and health supplements under India's FSSAI framework, with a permitted limit of Gum: 1-3 g; Bark: 5-10 g. Regulyze tracks its regulatory status, limits and label requirements across regulatory frameworks.
Regulatory status
| Framework | Status | Limit | Source | Last reviewed |
|---|---|---|---|---|
| India — FSSAI | Permitted | Gum: 1-3 g; Bark: 5-10 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.
Permitted dosage by form
| Preparation / form | Permitted daily quantity |
|---|---|
| Gum | 1-3 g |
| Bark | 5-10 g |
Per India's FSSAI Schedule listing for Babbul. Quantities are per-day permitted ranges for the stated form — confirm against the current official regulation for your product.
About Babbul
Babbul 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 Babbul permitted in nutraceuticals under FSSAI (India)?
Babbul 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 Babbul?
The permitted level recorded for Babbul is Gum: 1-3 g; Bark: 5-10 g. Limits can vary by product type and market — confirm against the current regulation.
What product category does Babbul belong to?
Babbul 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.