Diphenhydramine Citrate, Ibuprofen (diphenhydramine citrate, ibuprofen)

L. Perrigo Company · tablet, coated · NDC 0113-4007

Listed in the FDA National Drug Code directory

Diphenhydramine Citrate, Ibuprofen is a medicine made available by L. Perrigo Company, on the U.S. market since February 2009. Its listing category is "DRUG FOR FURTHER PROCESSING". Listing is not the same as FDA approval. A listing proves the product exists; it does not prove that a particular pack is genuine, so compare yours with the official description below.

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Recalls of this product

No FDA recalls are recorded for NDC 0113-4007. Recalls are listed in FDA enforcement reports from 2004 onward.

Most reported side effects for diphenhydramine citrate, ibuprofenReports to the FDA Adverse Event Reporting System (FAERS), all products with this ingredient
Fatigue8 reports
Nausea8 reports
Completed suicide5 reports
Abdominal distension4 reports
Diarrhoea4 reports
Hypoaesthesia4 reports
Insomnia4 reports
Joint swelling4 reports
Product use in unapproved indication4 reports
Vomiting4 reports
Show as table
ItemValue (reports)
Fatigue8
Nausea8
Completed suicide5
Abdominal distension4
Diarrhoea4
Hypoaesthesia4
Insomnia4
Joint swelling4
Product use in unapproved indication4
Vomiting4

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

Brand
Diphenhydramine Citrate, Ibuprofen
Generic name
diphenhydramine citrate, ibuprofen
Company
L. Perrigo Company
Form
tablet, coated
Route
—
Type
DRUG FOR FURTHER PROCESSING
Category
DRUG FOR FURTHER PROCESSING
Listing valid to
Dec 31, 2027
Product NDC
0113-4007

Active ingredients

Diphenhydramine Citrate
38 mg/1
Ibuprofen
200 mg/1

Packages (1)

The last part of the NDC identifies the pack size. Your box should show one of these.

0113-4007-00 1 bag in 1 drum (0113-4007-00) / 153840 tablet, coated in 1 bag

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.