BY Grace Zigah
The Food and Drugs Authority (FDA) has taken decisive action against Omama Herbal Mixture, revoking its marketing authorization due to the presence of dangerous prescription-only medicines. Laboratory tests revealed the product contained Diazepam, Metronidazole, Paracetamol, and Niacinamide, which are allopathic drugs not approved for use in registered herbal preparations.
These substances pose serious health risks to consumers, particularly when taken without prescription or advice from a qualified health professional.
The FDA emphasized that Omama Herbal Mixture was originally registered as a herbal remedy for malaria and loss of appetite, and the addition of these potent pharmaceutical substances was unauthorized.
The FDA has ordered an immediate halt to the sale and use of Omama Herbal Mixture and is working with Omama Herbal Group Limited to recall all affected batches from the market for safe disposal.
Regulatory and criminal proceedings have been initiated against individuals and entities behind the adulteration.
The FDA reaffirmed its commitment to protecting public health and maintaining the integrity of Ghana’s pharmaceutical and herbal markets.
Public Safety And Reporting
The public has been urged to report any individuals, pharmacies, or over-the-counter medicine sellers found offering Omama Herbal Mixture for sale to the nearest FDA office or via official hotlines.
