Advil PM (Ibuprofen and Diphenhydramine citrate)
Lil' Drug Store Products, Inc. · tablet, coated · NDC 66715-9633
Advil PM is an over-the-counter medicine made available by Lil' Drug Store Products, Inc., on the U.S. market since April 2022. It is marketed under an FDA approval (NDA NDA021394), 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.
What the genuine product looks like
From the official FDA label (version of Nov 27, 2024). Compare the colour, shape, imprint and packaging with what you have. Any difference is a reason to ask a pharmacist before taking it.
Product data on the label: Advil PM Ibuprofen and Diphenhydramine citrate CALCIUM STEARATE CARNAUBA WAX SILICON DIOXIDE STARCH, CORN CROSCARMELLOSE SODIUM FD&C BLUE NO. 2 ALUMINUM OXIDE GLYCERYL DIBEHENATE HYPROMELLOSE, UNSPECIFIED LACTOSE MONOHYDRATE MICROCRYSTALLINE CELLULOSE POLYDEXTROSE POLYETHYLENE GLYCOL, UNSPECIFIED SODIUM LAURYL SULFATE STEARIC ACID TITANIUM DIOXIDE IBUPROFEN IBUPROFEN DIPHENHYDRAMINE CITRATE DIPHENHYDRAMINE Capsule-Shaped, Smooth in texture w/ polish surface Advil;PM Advil PM Ibuprofen and Diphe…
Text on the package panel: Advil PM, 6ct, Lil' Drug Store ® - PDP/Package Advil ® PM Ibuprofen, 200 mg/ Diphenhydramine citrate, 38 mg Pain Reliever (NSAID)/ Nighttime Sleep-Aid [caplet image] 6 Coated Caplets* *Capsule-Shaped Tablets [ Lil' Drug Store ® logo] PDP/Package
What it is for
Active ingredients (in each caplet) Purposes Diphenhydramine citrate 38 mg Nighttime sleep-aid Ibuprofen 200 mg (NSAID) nonsteroidal anti-inflammatory drug Pain reliever
Key warnings
Warnings Allergy alert Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: hives facial swelling asthma (wheezing) shock skin reddening rash blisters If an allergic reaction occurs, stop use and seek medical help right away. Stomach bleeding warning This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you are age 60 or older have had stomach ulcers or bleeding problems take a blood thinning (anticoagulant) or steroid drug take other drugs containing prescription or nonprescription NSAIDs [a…
Excerpts from the FDA label. Always read the leaflet in your pack and ask a pharmacist or doctor about your own situation.
Recalls of this product
No FDA recalls are recorded for NDC 66715-9633. Recalls are listed in FDA enforcement reports from 2004 onward.
Show as table
| Item | Value (reports) |
|---|---|
| Drug ineffective | 2,823 |
| Pain | 1,964 |
| Nausea | 1,806 |
| Headache | 1,740 |
| Fatigue | 1,423 |
| Dizziness | 1,227 |
| Vomiting | 1,092 |
| Anxiety | 1,072 |
| Drug hypersensitivity | 1,047 |
| Diarrhoea | 939 |
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.