Diphenhydramine Hcl, Ibuprofen (diphenhydramine HCl, ibuprofen)

Catalent Pharma Solutions, LLC · capsule, liquid filled · NDC 11014-0018

Listed in the FDA National Drug Code directory

Diphenhydramine Hcl, Ibuprofen is a medicine made available by Catalent Pharma Solutions, LLC, on the U.S. market since December 2005. 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 11014-0018. Recalls are listed in FDA enforcement reports from 2004 onward.

Most reported side effects for diphenhydramine hcl, ibuprofenReports to the FDA Adverse Event Reporting System (FAERS), all products with this ingredient
Drug ineffective1,176 reports
Somnolence424 reports
Product use in unapproved indication346 reports
Drug effective for unapproved indication283 reports
Insomnia240 reports
Feeling abnormal220 reports
Fatigue182 reports
Dizziness177 reports
Intentional product misuse145 reports
Headache116 reports
Show as table
ItemValue (reports)
Drug ineffective1,176
Somnolence424
Product use in unapproved indication346
Drug effective for unapproved indication283
Insomnia240
Feeling abnormal220
Fatigue182
Dizziness177
Intentional product misuse145
Headache116

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 Hcl, Ibuprofen
Generic name
diphenhydramine HCl, ibuprofen
Company
Catalent Pharma Solutions, LLC
Form
capsule, liquid filled
Route
—
Type
DRUG FOR FURTHER PROCESSING
Category
DRUG FOR FURTHER PROCESSING
Listing valid to
Dec 31, 2027
Product NDC
11014-0018

Active ingredients

Diphenhydramine Hydrochloride
25 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.

11014-0018-1 1 bag in 1 box (11014-0018-1) / 8000 capsule, liquid filled 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.