RegulyzeDisodium Uridine 5-monophosphate salt
Disodium Uridine 5-monophosphate salt is a nucleotide 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 Disodium Uridine 5-monophosphate salt
Disodium Uridine 5-monophosphate salt is tracked in the Regulyze Ingredient Intelligence database as a nucleotide. 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 Disodium Uridine 5-monophosphate salt permitted in nutraceuticals under FSSAI (India)?
Disodium Uridine 5-monophosphate salt 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 Disodium Uridine 5-monophosphate salt?
No single numeric limit is listed in the source for Disodium Uridine 5-monophosphate salt; permitted use is at GMP or as specified. Confirm against the current regulation.
What product category does Disodium Uridine 5-monophosphate salt belong to?
Disodium Uridine 5-monophosphate salt is classified under: Nucleotides.
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.