Homoeopathic medicines
Understand the requirements to import, manufacture or sell homoeopathic medicines in Singapore.
Last updated 7 May 2026
What is a homoeopathic medicine
Homoeopathic medicine (HM) refers to a medicine that is formulated for use on the principle of "like cures like". It means any substance used in the system of therapeutics in which a disease is treated by the use of minute amounts of one or more substances which, in their undiluted forms, are capable of producing in a healthy human being symptoms similar to those of the disease being treated. It is prepared to a homoeopathic manufacturing procedure described by a Homoeopathic pharmacopoeia1.
Food and supplements of food nature come under the purview of the Singapore Food Agency (SFA). View the interactive Food-Health Product Classification Tree for more information.
1 List of recognised Homoeopathic Pharmacopoeias:
Homoeopathic Pharmacopoeia of the United States (HPUS)
Homoeopathic ArzneiBuch (HAB) or German Homoeopathic Pharmacopoeia (GHP)
Pharmacopée Française or French Pharmacopoeia (PhF)
European Pharmacopoeia (Ph.Eur.)
Encyclopedia of Homoeopathic Pharmacopoeia (EHP)
Is my product a complementary health product (CHP)?
Answer a few questions in our self-help tool to find out if your product is considered a complementary health product (e.g. Chinese Proprietary Medicine, Health Supplement, Traditional Medicine) in Singapore. You can also get a print-out of your product classification outcome from the tool.
Want to know more about CHP product classification? Click here for our FAQ.
Regulatory requirements of HM
HM are not subject to approvals and licensing by HSA for their importation, manufacture and sales. HSA prohibits the addition of medicinal ingredients such as steroids in HM. HSA also sets strict limits on toxic heavy metals in these products. Dealers (importers, manufacturers, wholesale dealers and sellers) have the obligation to ensure that their products are not harmful or unsafe, and that they conform with the following guidelines before supplying HM into Singapore.
Toxic heavy metal limits
Your product must not exceed the following:
List of permissible heavy metal limits
Heavy metal | Permissible limits |
|---|---|
Arsenic | 5 parts per million (ppm) |
Cadmium | 0.3ppm |
Lead | 10ppm |
Mercury | 0.5ppm |
Microbial limits
Your product must not exceed the following microbial limits:
Oral products
List of microbe and microbial limits
Microbe | Microbial limits |
|---|---|
Total aerobic microbial count | Not more than 105 CFU per g or ml |
Yeast and mould count | Not more than 5 x 102 CFU per g or ml |
Escherichia coli, Salmonellae and Staphylococcus aureus | Absent in 1g or ml |
Topical products
List of microbe and microbial limits
Microbe | Microbial limits |
|---|---|
Total aerobic microbial count | Not more than 104 CFU per g or ml |
Yeast and mould count | Not more than 5 x 102 CFU per g or ml |
Pseudomonas aeruginosa and Staphyloccocus aureus | Absent in 1g or ml |
Notwithstanding the limits stated above, it is the obligation of the dealers and sellers to ensure that the microbial content and heavy metals of the product is appropriate and safe when used according to the recommended conditions of use and target users.
Labelling requirements
Your product label should include the ingredients and their strengths in English. You are also not allowed to claim or indirectly suggest that the product will prevent, alleviate or cure any of the following conditions:
Blindness
Cancer
Cataract
Drug addiction
Deafness
Diabetes
Epilepsy or fits
Hypertension
Insanity
Kidney diseases
Leprosy
Menstrual disorder
Paralysis
Tuberculosis
Sexual function
Infertility
Impotency
Frigidity
Conception and pregnancy
Dealers must ensure that all health claims and information associated with the products are sufficiently supported and submitted to HSA as and when required. Otherwise, all unsubstantiated health claims and information will be considered misleading and must be removed from the product materials.
Prohibited ingredients
HM manufactured or imported and sold here cannot contain these ingredients or substances:
Synthetic drugs
Transmissible Spongiform Encephalopathy (TSE)
Animal derived ingredients
Transmissible spongiform encephalopathy (TSE) refers to a group of progressive diseases including scrapie in sheep and goats, chronic wasting disease in mule, deer and elk, bovine spongiform encephalopathy (BSE) in cattle, as well as Kuru and Creutzfeldt-Jakob Disease (CJD) in humans.
The infectious agents causing these diseases replicate and cause neurological disorders and eventual death in the infected individuals. There are currently no early diagnostic tests or known therapies for these diseases.
If your product contains animal derived ingredients, you must comply with our TSE guidelines to minimise the risk of TSE transmission.
Substances from endangered species
If your product contains substances from endangered species listed under the Endangered Species (Import & Export) Act, you should contact the Wildlife Management Group of NParks to obtain the necessary Convention on the International Trade in Endangered Species of Wild Fauna and Flora (CITES) import and export permits.
Advertisements and promotions
You will require a valid permit from us before publishing any medical advertisement or conducting any sales promotion activity directed at the general public.
Refer to our advertisements and promotions guidelines for more information on what is required before you run any advertisement or promotion for your products.
To complement the traditional medicines, homoeopathic medicines, MOB and medicated plasters Guidelines, a list of questions and answers on the controls, safety and quality, claims and labelling can be found here
Free Sale Certificate (FSC)
Some importing countries may require a certificate to show that the product is currently sold and distributed in Singapore.
As such, local exporters may apply for a FSC from the Health Sciences Authority.
Each FSC is specific to one product and allows the inclusion of up to five importing countries. Information in the FSC includes:
Name of product
Importing countries
Name and address of the manufacture(s) and distributor(s)
Intended use
Ingredients
Date of Issue of the FSC
With effect from 25 March 2026, HSA will be issuing verifiable electronic certificates for exporters (including Certificate of a Pharmaceutical Product and Free Sale Certificate) using GovTech's FileSG digital platform. FileSG will replace TrustDocs for issuance of verifiable electronic documents. There will not be any changes to the application fees for these certificates. For further information, please refer to the HSA Frequently Asked Questions on Migration of TrustDocs to FileSG.