In a regulatory filing, the company stated that the EIR was issued following a good manufacturing practice (GMP) inspection conducted by the USFDA. The inspection outcome has been classified as ...

The Food and Drug Administration announced the recall of tens of thousands of cases of deodorant. The FDA said that it was ...

The Food and Drug Administration has recalled more than 67,000 cases of deodorant sold at major retailers due to manufacturing practices that violate federal regulations. Three types of Power Sticks ...

More than 67,000 Power Stick deodorants have been recalled across the US after the FDA flagged serious manufacturing ...

Three roll-on deodorant products were recalled earlier this month due to deviations from regulations on manufacturing set by ...

Three roll-on deodorant products were recalled earlier this month due to deviations from regulations on manufacturing set by ...

A.P. Deauville, a Pennsylvania-based health and beauty manufacturer, has recalled more than 67,000 cases of its Power Stick ...

Three roll-on deodorant products were recalled earlier this month due to deviations from regulations on manufacturing set by ...

Three roll-on deodorant products were recalled earlier this month due to deviations from regulations on manufacturing set by ...

In a recent announcement, the U.S. Food and Drug Administration (FDA) has raised concerns among consumers by issuing a ...

In a move to reduce dependence on imported medicines, the Federal Government has launched a comprehensive Good Manufacturing ...