Class II · Moderate risk
Guaifenesin DM Cherry liquid
Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin DM liquid due incorrect dose markings on the dosing cups.
National Drug Code
Is NDC 49348-0828-34 recalled?
Guaifenesin DM Cherry liquid
Yes — this exact package was recalled
1 FDA recall names the code 49348-0828-34 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 49348-0037 Sunmark Eye Drops Original Formula 3
- 49348-0109 See recall 2
- 49348-0136 See recall 2
- 49348-0001 See recall 1
- 49348-0410 See recall 1
- 49348-0543 Loratadine and Pseudoephedrine Sulfate 1
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