ibuprofen pm (diphenhydramine citrate, ibuprofen)
Publix Super Markets Inc · tablet, film coated · NDC 56062-050
ibuprofen pm is an over-the-counter medicine made available by Publix Super Markets Inc, on the U.S. market since September 2011. It is marketed under an FDA approval (ANDA ANDA079113), so the FDA has reviewed its safety, effectiveness and manufacturing. A listing proves the product exists; it does not prove that a particular pack is genuine, so compare yours with the official description below.
Recalls of this product
No FDA recalls are recorded for NDC 56062-050. Recalls are listed in FDA enforcement reports from 2004 onward.
Show as table
| Item | Value (reports) |
|---|---|
| Fatigue | 8 |
| Nausea | 8 |
| Completed suicide | 5 |
| Abdominal distension | 4 |
| Diarrhoea | 4 |
| Hypoaesthesia | 4 |
| Insomnia | 4 |
| Joint swelling | 4 |
| Product use in unapproved indication | 4 |
| Vomiting | 4 |
These counts are reports, not proof that the medicine caused the problem. Popular medicines get more reports simply because more people take them. They are useful for spotting what to watch for, not for comparing medicines.
Official listing
Active ingredients
Packages (1)
The last part of the NDC identifies the pack size. Your box should show one of these.
Think your pack is fake?
Stop taking it, keep the pack and receipt, and show it to a pharmacist. In the U.S., report it to FDA MedWatch; elsewhere, to your national medicines regulator. How to spot a fake medicine.
Source: openFDA (U.S. Food and Drug Administration) drug directory, labels, enforcement reports and FAERS, retrieved Nov 8, 2026. The FDA notes this data should not be relied on alone for medical decisions. Not medical advice.