Is RIBOFLAVIN safe in cosmetics?
RIBOFLAVIN has a safety rating of "GOOD" in our database. EU status: permitted. US status: permitted. 3 toxicological study endpoint(s) are available in our database.
Also known as: Riboflavin (vitamin B2), Vitamin B2 (riboflavin), Aqua-Flave, Benzo(g)pteridine-2,4(3H,10H)-dione, 7,8-dimethyl-10-(D-ribo-2,3,4,5-tetrahydroxypentyl)-, Dermadram (+15 more)
RIBOFLAVIN (CAS 83-88-5) is a cosmetic colorant functioning as Colorant (CI 75170, yellow); antioxidant co-factor; skin conditioning. NOAEL 160 mg/kg bw/day (cross-referenced against ToxValDB ECHA IUCLID); EU Regulation 1223/2009 status: permitted. Industrial safety data is also available in the chemical safety database. Same-CAS public records also appear in industrial chemical safety, pharmaceutical, and food safety data.
For full compliance data across multiple jurisdictions, use the Substance Compliance tool.
Margin of Safety, dermal absorption, and sensitization profile summaries for RIBOFLAVIN.
Calculate MoS for your specific formulation with the MoS Calculator.
3 study endpoints found for RIBOFLAVIN. NOAEL (No Observed Adverse Effect Level) values are used to calculate the Margin of Safety per SCCS methodology.
| Endpoint | Value | Route | Species | Study Type | Source |
|---|---|---|---|---|---|
| NOAEL | 25 mg/kg bw/day | oral | dog | Subchronic | COSMOS DB |
| NOAEL | 50 mg/kg bw/day | oral | rat | Multigeneration Reproductive | COSMOS DB |
| NOAEL | 400 mg/kg bw/day | oral | mouse | Short Term Toxicity | COSMOS DB |
Globally Harmonized System classification per ECHA C&L inventory and ILO/WHO International Chemical Safety Cards.
Pre-calculated NOAEL → SED → MoS audit trail for RIBOFLAVIN across SCCS product categories, with measured dermal absorption where available.
4 toxicity values from EPA ToxValDB (aggregated from CCTE, HPV, ToxRefDB, IRIS, and other regulatory dossiers).
| Endpoint | Value | Species | Route | Duration | Source |
|---|---|---|---|---|---|
| NOAEL | =160 mg/kg-day | Rat | oral | subchronic | EFSA |
| ADI | <=0.5 mg/kg | Human | oral | - | WHO/JECFA |
| LD50 | >10000 mg/kg | Rat | oral | - | ChemIDplus |
| LD50 | >40000 mg/kg | Rat | oral | - | ECHA |
European Chemicals Agency REACH dossier and Substances of Very High Concern listing.
Additional regulatory detail beyond the 7-jurisdiction summary: Saudi SFDA, Korea MFDS, ASEAN ACD, Japan/Korea, Brazil/India, and cross-jurisdictional restriction entries.
| Jurisdiction | Status | Max % | Product Type |
|---|---|---|---|
| CN | permitted_colorant | - | All cosmetics (Class 1) |
Preliminary editorial summary for RIBOFLAVIN — not a computed safety verdict. See the sourced toxicological data above.
Public NOAEL study rows linked to RIBOFLAVIN by CAS number or substance name.
Same-CAS public records found in pharmaceutical and food safety data.
Same-CAS rows from the pharmaceutical spoke database.
Same-CAS food additive or FDA GRAS records from the core public database.
RIBOFLAVIN has a safety rating of "GOOD" in our database. EU status: permitted. US status: permitted. 3 toxicological study endpoint(s) are available in our database.
RIBOFLAVIN EU regulatory status: permitted. This is based on EU Regulation 1223/2009 and its amendments.
RIBOFLAVIN functions as: Colorant (CI 75170, yellow); antioxidant co-factor; skin conditioning. It is classified as a Colorant in our database. CAS number: 83-88-5.
The NOAEL (No Observed Adverse Effect Level) for RIBOFLAVIN is 25 mg/kg bw/day based on a Subchronic study via oral route in dog. A total of 3 study endpoints are available. Source: COSMOS DB.
RIBOFLAVIN also appears in industrial chemical safety, pharmaceutical, and food safety data. The cross-vertical cards on this page render same-CAS public rows from the matched databases.
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