About
Haritaki is the dried fruit of Terminalia chebula Retz. (family Combretaceae), a medium-sized deciduous tree native to South and Southeast Asia, widely distributed in India up to 1500 m altitude. It has been used for centuries in Ayurvedic, Unani, Siddha, and Tibetan medicine as a digestive tonic, laxative, antimicrobial, and antioxidant agent, and is a principal constituent of the classic Ayurvedic formulation Triphala.
Safety summary
Haritaki is generally well tolerated in traditional and short-term clinical use; a randomized crossover trial in healthy volunteers found a single oral dose of 1000 mg was well tolerated with no adverse events recorded. Its high hydrolysable tannin content (chebulic acid, chebulinic acid, chebulagic acid, gallic acid) may inhibit iron and mineral absorption with prolonged or high-dose use, and large doses may exert pronounced laxative or purgative effects. No formal Acceptable Daily Intake (ADI) has been established by any major regulatory authority (EFSA, FDA, JECFA), and safety data for pregnancy, lactation, and paediatric populations remain insufficient.
Regulatory landscape
| Jurisdiction | Status | Note |
|---|---|---|
| FSSAI (Food Safety and Standards Authority of India) (India) | Approved | Permitted as a botanical/herbal ingredient under FSS (Health Supplements, Nutraceuticals, Food for Special Dietary Use, Food for Special Medical Purpose, Functional Foods and Novel Foods) Regulations, 2016. Recognised as a traditional Ayurvedic herb; no specific maximum daily dose fixed for food use. Products making health claims must comply with FSSAI claim guidelines.source |
| EFSA (European Food Safety Authority) (European Union) | Under_review | Terminalia chebula is not listed as an approved novel food or food supplement ingredient in the EU Novel Food Catalogue. Any use as a food ingredient or supplement in the EU would require a novel food safety authorisation under Regulation (EU) 2015/2283 prior to placement on the market.source |
| FDA (Food and Drug Administration) (United States) | Under_review | Not listed as an approved food additive or GRAS substance in 21 CFR Parts 172, 182, or 184. Commercially marketed in the US as a dietary supplement ingredient under DSHEA (21 USC §321(ff)); no food additive petition or GRAS notice for direct food use identified in FDA records.source |
Who should approach with care
Research citations
- 1PubMed. Haritaki (Chebulic myrobalan) and its varieties. pmc.ncbi.nlm.nih.gov
- 2PubMed. A randomized, double-blind, placebo-controlled, cross-over study to evaluate analgesic activity of Terminalia chebula in healthy human volunteers using a mechanical pain model. ncbi.nlm.nih.gov
- 3PubMed. A Review on Potential Mechanisms of Terminalia chebula in Alzheimer's Disease. pmc.ncbi.nlm.nih.gov
- 4PubMed. A comprehensive review on the diverse pharmacological perspectives of Terminalia chebula Retz, 2022. pubmed.ncbi.nlm.nih.gov
- 5PubMed. Hypolipidemic activity of haritaki (Terminalia chebula) in atherogenic diet induced hyperlipidemic rats, 2010. pubmed.ncbi.nlm.nih.gov
