In brief
On 27 April 2022, the Health Sciences Authority (HSA) announced that it detected potent medical ingredients in two products that were marketed on local e-commerce and social media platforms. The HSA has since removed the affected listings and issued warnings to sellers of said products.
Key takeaways
- While there is currently no registration or licensing requirements in relation to the import, manufacture or sales of health supplements, dealers must comply with the HSA’s safety and quality standards. The addition of such medical ingredients is prohibited, and there are strict toxic heavy metal, microbial, vitamin and mineral limits.
- Anyone found to have supplied products that are adulterated may be imprisoned for up to three years and/or fined up to SGD 100,000 upon conviction.
- In its recently revised health supplements regulatory framework, the HSA also introduced further clarity on the labelling standards and scope of permissible claims for health supplements. Health supplements must contain the labelling information set out in the Guidelines for Labelling Standards of Traditional Medicines and Health Supplements (“Labelling Guidelines“). Additionally, the Guidelines for Claims and Claims Substantiation of Traditional Medicines and Health Supplements set out a list of general principles that all claims must adhere to, including a requirement for claims to truthfully state the nature, quality and properties of the health supplement, and a prohibition against any claim that a product has no side effects. We cover the HSA’s updated health supplements framework in greater detail here.
Background
On 27 April 2022, the Health Sciences Authority (HSA) announced that it detected potent medical ingredients in two products that were marketed on local e-commerce and social media platforms. The HSA has since removed the affected listings and issued warnings to sellers of said products.
The first product was marketed as a sexual enhancement supplement and made claims that it was “devoid of animal element, devoid of stimulants, devoid of side effects”. The product was found to contain up to over 60 times the usual dose of tadalafil, a prescription-only medicine that may pose serious risks to individuals with heart-related problems and cause serious adverse side effects, such as heart attacks or palpitations, if used inappropriately.
The second product was marketed as a ‘new and improved’ version of a weight loss supplement that the HSA previously flagged in 2021. The product notably lacked key information required by the Labelling Guidelines, such as proper use directions and manufacturing information. The product also contained misleading marketing claims. Like its predecessor, the HSA detected high levels of sibutramine in the product, a substance that has been banned in Singapore since 2010 due to its role in increasing the risk of stroke and heart attack.
Sellers have been directed to stop the sale of affected products immediately.
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