Current location:home page > Laws and regulations

UK food agency warns against DMAA

admin2 weeks ago (05-19)Laws and regulations46
High blood pressure, nausea, cerebral haemorrhage, stroke and death were among the health issues ref…
High blood pressure, nausea, cerebral haemorrhage, stroke and death were among the health issues referenced. The agency warned people who might have taken it to visit a doctor.


The FSA said it was working with enforcement authorities to remove DMAA (methylhexanamine/1,3-dimethylamylamine) products from shelves, even as it confirmed that the regulatory status of the ingredient remained unresolved in the UK.

A spokesperson said that determination was in the hands of the Medicines and Healthcare products Regulatory Agency (MHRA), even though the MHRA already warned several retailers (mostly online) to remove DMAA products like USPLabs’ Jack3D at the beginning of the year.

“If they decide it is a food supplement then we will decide which regulations are appropriate for it,”
 the spokesperson said.

MHRA activity

While regulators around the world are condemning the stimulant that many manufacturers have been claiming is derived from the geranium plant and therefore suitable as a food supplement ingredient, the FSA said it would take no further action until the MHRA completed its own investigation, apparently now into one particular product.

“An independent advisory panel has been asked by the MHRA to advise whether a certain product containing DMAA should be classed as an unlicensed medicine and therefore subject to medicine controls,” 
the FSA wrote in yesterday’s missive.

“This advice may also have implications for the status of other DMAA-containing supplements.”

The MHRA would not confirm which product was under investigation, when that investigation was likely to conclude, nor why it had already issued warning letters to DMAA retailers without officially determining its status.

In recent weeks Australia’s medicines agency – the Therapeutic Goods Administration (TGA) – placed DMAA on a poisons list, joining New Zealand, most of Scandinavia, France, Ireland and other nations in acting against a stimulant that has caused more positive doping tests for elite athletes in recent years than any other substance.

When the MHRA sent its initial round of letters one online retailer – Predator Nutrition – said the agency told it to to remove a host of products containing a long list of ingredients including synephrine, yohimbe, milk thistle, valerian, GABA and DHEA.

标签: DMAAMHRATGAFSA

Related articles

FSSAI recommends 20 RAFT manufacturers’ applications for final approval

FSSAI has recommended 20 applications of manufacturers of Rapid Food Testing Kits (RAFT) for final a…

Regulations on Food Irradiation in China

Regulations on Food Irradiation in China

Food irradiation is a new type of preservation technology. It has been widely used in food steriliza…

Soil Association revises organic standards

Organic certification body Soil Association has thoroughly review the  current organic standards in…

Ukraine adopts law regulating food labelling

Ukraine has taken another step in approximation with EU legislation, this time in the area of inform…

Reviewing sesame labeling regulations: FDA examines prevalence and severity of sesame allergies

The US Food & Drug Administration (FDA) is investigating the prevalence and severity of sesame a…

EU mulls regulation changes for raw juices and Listeria in sprouted seeds

Leaders of the European Union are looking at changing regulations around unpasteurized juices and Li…