Aloe Vera
Aloe vera · Sap/gel
Aloe Vera (Aloe vera) is a nutraceutical permitted for use in nutraceuticals and health supplements under India's FSSAI framework. Regulyze tracks its regulatory status, limits and label requirements across regulatory frameworks.
Regulatory status
| Framework | Status | Limit | Source | Last reviewed |
|---|---|---|---|---|
| India — FSSAI | Permitted | As specified / GMP | 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 Aloe Vera
Aloe Vera is tracked in the Regulyze Ingredient Intelligence database as a nutraceutical (Aloe vera). 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 Aloe Vera permitted in nutraceuticals under FSSAI (India)?
Aloe Vera (Aloe vera) (listed in the regulation as “Aloe vera juice/concentrate/powder of sap/gel”) 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 Aloe Vera?
No single numeric limit is listed in the source for Aloe Vera; permitted use is at GMP or as specified. Confirm against the current regulation.
What product category does Aloe Vera belong to?
Aloe Vera is classified under: Nutraceuticals, Botanicals.
What is the botanical (scientific) name of Aloe Vera?
Aloe Vera corresponds to Aloe vera, with the sap/gel 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.
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