NOAEL Studies
Cosmetic Ingredient
Basic Red 51 NOAEL Studies
INCI: BASIC RED 51
CAS: 77061-58-6
Raw No Observed Adverse Effect Level endpoint records grouped by source. This page does not render calculated Margin of Safety values.
COSMOS DB 1 endpoint
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| COSMOS DB | LOAEL | 10 | mg/kg bw/day | rat | oral | 91 day | Subchronic | SCCS; RCC Project 681322. (1998). Subchronic 13-week oral toxicity (feeding) study in therat |
SCCNFP Opinion 7 endpoints
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| SCCNFP Opinion | NOAEL | =10 | mg/kg/day | - | dermal | Sub-chronic | repeated dose toxicity | Ref : 5 2, p.10 |
| SCCNFP Opinion | NOAEL | =10 | mg/kg bw/day | - | oral | sub-chronic | repeated dose toxicity | p.20 |
| SCCNFP Opinion | NOAEL | =12.25 | mg/kg | rat | dermal | 4 weeks | repeated dose toxicity | Ref : 4 2, p.8 |
| SCCNFP Opinion | NOAEL | =12.25 | mg/kg bw/day | - | oral | sub-chronic | repeated dose toxicity | Ref. : 10 2, p.20 |
| SCCNFP Opinion | NOAEL | =20 | mg/kg bw/day | human | - | - | developmental toxicity | Ref. : 11 2, p.13 |
| SCCNFP Opinion | NOAEL | =50 | mg/kg | - | dermal | Sub-chronic | repeated dose toxicity | Ref : 5 2, p.10 |
| SCCNFP Opinion | NOAEL | =180 | mg/kg bw/day | human | - | - | developmental toxicity | Ref. : 11 2, p.13 |
SCCS Opinion 9 endpoints
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| SCCS Opinion | NOAEL | =0.005 | mg/kg | rat | oral | subchronic | repeated dose toxicity | p.29 |
| SCCS Opinion | NOAEL | =0.006 | mg/kg | rat | oral | subchronic | repeated dose toxicity | p.28 |
| SCCS Opinion | NOAEL | =10 | mg/kg bw/day | - | - | Chronic | genotoxicity | p.18 |
| SCCS Opinion | NOAEL | =10 | mg/kg bw | rat | oral | subchronic | repeated dose toxicity | p.28 |
| SCCS Opinion | NOAEL | =12.25 | mg/kg | rat | dermal | 14 days | repeated dose toxicity | p.16 |
| SCCS Opinion | NOAEL | =20 | mg/kg bw/day | mouse | oral | - | developmental toxicity | p.24 |
| SCCS Opinion | NOAEL | =50 | mg/kg bw/d | - | - | Chronic | genotoxicity | p.18 |
| SCCS Opinion | NOAEL | =180 | mg/kg bw/day | mouse | oral | - | developmental toxicity | p.24 |
| SCCS Opinion | NOAEL | =2000 | mg/kg bw | - | oral | sub-chronic | repeated dose toxicity | p.28 |
ECHA 2 endpoints
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| ECHA | NOEL | =20 | mg/kg bw/day | Rat | oral | - | reproduction developmental | QUALITY=4 (not assignable); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7d1cfe4b0a7c65d2303c5; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/23102/7/9/3?documentUUID=b65d9bd1-9885-419b-b112-cd6d2ae0cdc2; YEAR=2017; ORIGINAL_YEAR=2017; TOXICOLOGICAL_EFFECT=maternal: body weight and weight gain|maternal: clinical signs|maternal: food consumption and compound intake|maternal: mortality|maternal: pre and post implantation loss; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical signs|food and/or water consumption|mortality/survival|reproduction; STUDY_GROUP=ECHA IUCLID:15822261:F:-maternal; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_ef1a90d88e9e3dca57ca90c10aefd919 |
| ECHA | NOEL | =180 | mg/kg bw/day | Rat | oral | - | developmental | QUALITY=4 (not assignable); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7d1cfe4b0a7c65d2303c5; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/23102/7/9/3?documentUUID=b65d9bd1-9885-419b-b112-cd6d2ae0cdc2; YEAR=2017; ORIGINAL_YEAR=2017; TOXICOLOGICAL_EFFECT=fetus: changes in sex ratio|fetus: fetal/pup body weight changes|fetus: skeletal malformations; TOXICOLOGICAL_EFFECT_CATEGORY=development; STUDY_GROUP=ECHA IUCLID:15820918:-:-fetal; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_a9d87503c7bb4089862f29569b6f597a |
Regulatory source 20 endpoints
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| Regulatory source | developmental toxicity | 20 | mg/kg bw/day | human | - | - | developmental toxicity | p.13 |
| Regulatory source | developmental toxicity | 180 | mg/kg bw/day | human | - | - | developmental toxicity | p.13 |
| Regulatory source | repeated dose toxicity | 10 | mg/kg/day | - | dermal | Sub-chronic | repeated dose toxicity | p.10 |
| Regulatory source | repeated dose toxicity | 10 | mg/kg bw/day | - | dermal | Sub-chronic | repeated dose toxicity | p.10 |
| Regulatory source | repeated dose toxicity | 10 | mg/kg bw/day | - | oral | sub-chronic | repeated dose toxicity | p.20 |
| Regulatory source | repeated dose toxicity | 12.25 | mg/kg | rat | dermal | 4 weeks | repeated dose toxicity | p.8 |
| Regulatory source | repeated dose toxicity | 12.25 | mg/kg bw/day | - | oral | sub-chronic | repeated dose toxicity | p.20 |
| Regulatory source | repeated dose toxicity | 20 | mg/kg bw/day | - | oral | sub-chronic | repeated dose toxicity | p.20 |
| Regulatory source | repeated dose toxicity | 50 | mg/kg | - | dermal | Sub-chronic | repeated dose toxicity | p.10 |
| Regulatory source | developmental toxicity | 20 | mg/kg bw/day | mouse | oral | - | developmental toxicity | p.24 |
| Regulatory source | developmental toxicity | 20 | mg/kg bw/day | - | - | - | developmental toxicity | p.24 |
| Regulatory source | developmental toxicity | 180 | mg/kg bw/day | mouse | oral | - | developmental toxicity | p.24 |
| Regulatory source | developmental toxicity | 180 | mg/kg bw/day | - | - | - | developmental toxicity | p.24 |
| Regulatory source | genotoxicity | 10 | mg/kg bw/day | - | - | Chronic | genotoxicity | p.18 |
| Regulatory source | genotoxicity | 50 | mg/kg bw/d | - | - | Chronic | genotoxicity | p.18 |
| Regulatory source | repeated dose toxicity | =0.005 | mg/kg | rat | oral | subchronic | repeated dose toxicity | p.29 |
| Regulatory source | repeated dose toxicity | =0.006 | mg/kg | rat | oral | subchronic | repeated dose toxicity | p.28 |
| Regulatory source | repeated dose toxicity | =10 | mg/kg bw | rat | oral | subchronic | repeated dose toxicity | p.28 |
| Regulatory source | repeated dose toxicity | 12.25 | mg/kg | rat | dermal | 14 days | repeated dose toxicity | p.16 |
| Regulatory source | repeated dose toxicity | 2000 | mg/kg bw | - | oral | sub-chronic | repeated dose toxicity | p.28 |
openFDA substances 1 endpoint
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| openFDA substances | FDA UNII substance identifier | A7A946JJ6I | UNII | - | - | - | chemical | - |