Acute oral toxicity data of a test substance is used to satisfy hazard classification and labelling requirements for its risk
assessment in human health and environment (OECD, 2001b).
In the present study, acute oral toxicity assessment of KalmColdTM did not cause mortality, abnormal clinical signs or any significant pathological changes up to the dose level of 5000 mg/kg body weight.
Also, the overall body weight gain was found to be normal in all the treated rats and hence resulted in labelling
KalmColdTM as unclassified in the hazard category according to