Cytotoxicity test for the identification of substances with acute oral toxicity LD50>2000 mg/kg

Regulatory reference: OECD 129: on using cytotoxicity tests to estimate starting doses for acute oral systemic toxicity tests;
EURL-ECVAM 2011: follow-up study on the predictive capacity of the 3T3 Neutral Red Uptake cytotoxicity assay to correctly identify substances not classified for acute oral toxicity under the EU CLP system.
Claim: Biocompatible and Non citotoxic
Application field: Chemical substances or mixtures.
Description of the test: The in vitro LD50 prediction test is designed to test chemicals or mixtures by evaluating their cytotoxic effect on an in vitro model of BALB/c 3T3 murine fibroblasts.
Posted in Non citotoxic, Cosmetic raw materials, Claim for cosmetics, Biocompatible