Research / Safety

Safety Profile & Toxicology

Turmesac® is a full-spectrum phytochemical composition derived from turmeric rhizome and manufactured by Star Hi Herbs Pvt. Ltd. Its safety has been evaluated through acute and repeated-dose preclinical toxicity studies, with no mortality or Turmesac®-related toxic effects at the tested doses.

01 / Acute

Acute oral toxicity

2,000mg/kg highest tested single dose
0Mortality reported
5Dose levels evaluated
NormalBody weight and intake

Turmesac® was evaluated at oral doses of 50, 250, 500, 1,000 and 2,000 mg/kg body weight. At the highest tested dose of 2,000 mg/kg:

  • No acute toxic symptoms were observed
  • No mortality occurred
  • Body weight remained within the normal range
  • Food and water intake remained normal
  • No abnormal clinical signs were reported
  • Relative organ weights showed no Turmesac®-related changes
02 / Sub-acute

28-day repeated-dose toxicity

A sub-acute toxicity study evaluated daily oral administration of Turmesac® at 250, 500 and 1,000 mg/kg body weight per day for 28 days. No Turmesac®-related toxic effects were detected at any tested dose. Evaluated safety parameters included:

  • General behaviour and clinical signs
  • Mortality
  • Body-weight development
  • Food and water consumption
  • Relative organ weights
  • Hematological parameters
  • Biochemical parameters
  • Gross and microscopic organ histopathology

The treated groups showed no significant differences from the control group. Histopathological examination found normal tissue architecture in the evaluated organs. These findings support a broad preclinical safety margin across the tested dose range.

03 / Cellular

Cellular safety observations

Additional in-vitro studies provide supportive cellular safety information, although they do not replace formal toxicology testing.

In-vitro studies on MCF-7 (breast cancer cell line) and HeLa (cervical cancer cell line) showed efficient anticancer activity of Turmesac®, with IC₅₀ values of 163.19 µg/mL and 115.12 µg/mL respectively. A dose-dependent decrease in cell viability was reported for both cell lines upon treatment with Turmesac®.

04 / Quality

Heavy metals and contaminants

Specification limits and batch-testing results for lead, arsenic, cadmium, mercury, pesticide residues, aflatoxins, microbiological contaminants and residual solvents are provided from the current specification sheet and batch-specific Certificate of Analysis on request.

05 / Regulatory

Regulatory considerations

Turmesac® is intended for use as an ingredient in appropriately formulated products. The information on this page summarizes preclinical research and does not establish that Turmesac® diagnoses, treats, cures or prevents any disease. Safety, permitted use levels, labelling and claims must be assessed according to the regulations of each destination market.

06 / FAQ

Safety questions

Is Turmesac® safe?

Preclinical studies reported no mortality at a single oral dose of 2,000 mg/kg and no Turmesac®-related toxic effects during a 28-day study at doses up to 1,000 mg/kg/day.

Does Turmesac® have known side effects?

No Turmesac®-related toxic effects were reported in acute and 28-day animal studies. The available evidence is preclinical and does not establish the incidence of side effects in humans.

Request the Turmesac® safety and technical dossier

Toxicology reports, specifications and regulatory documentation are available to qualified partners.