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In November 2010, Mylanta was voluntarily recalled [2] due to what is described as some labelling concerns. According to sources within the company at that time, these concerns stemmed from the fact that small traces of alcohol were found in the flavoring agents of the liquid version of the antacid which was not disclosed on the labelling itself, and that the problem would be rectified "shortly".
Now it's dragging Merck (MRK) with it as the two announced a recall of 12 over-the-counter Mylanta heartburn. If you get the feeling Johnson & Johnson (JNJ) is recalling products every day, you ...
Johnson & Johnson-Merck Consumer Pharmaceuticals Co. recalled 12 million bottles of Mylanta and thousands of packages of AlternaGel because flavoring used in the products contains a small amount ...
Here is the recall roundup from the past. Skip to main content. Sign in. Mail. 24/7 Help. For premium support please call: 800-290-4726 more ways to reach us. Mail. Sign in. Subscriptions ...
In August 2013, there was a recall of Maalox products. [12] "The recall encompasses 9 different types of its Maalox chewable tablets, including more than 3.4 million bottles of Maalox Advanced Maximum Strength Antacid & Antigas." [13] They planned to restart production on a line-by-line basis, but the Maalox line had not by then been restarted ...
The 2010 Johnson & Johnson children's product recall involved 43 over-the-counter children's medicines announced by McNeil Consumer Healthcare, a subsidiary of Johnson & Johnson, on April 30, 2010. Medications in the recall included liquid versions of Tylenol , Tylenol Plus, Motrin , Zyrtec , and Benadryl .
This searchable list includes products in the meat recall due to possible listeria contamination sold at Aldi, Trader Joe's, Wegmans, Walmart, others.
Known as the "JV," this 50/50 joint venture between Johnson & Johnson and Merck handled the OTC product lines Pepcid, Mylanta, and Mylicon and is located at the McNeil Consumer Healthcare headquarters in Fort Washington, Pennsylvania.