Physicians Care Ibuprofen (Ibuprofen 200mg)
Acme United Corporation · tablet, film coated · NDC 0924-0076
Physicians Care Ibuprofen is an over-the-counter medicine made available by Acme United Corporation, on the U.S. market since February 2016. It is marketed under an FDA approval (ANDA ANDA079174), 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 Oct 31, 2025). 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: Physicians Care Ibuprofen Ibuprofen 200mg IBUPROFEN IBUPROFEN STARCH, CORN STEARIC ACID TITANIUM DIOXIDE SODIUM STARCH GLYCOLATE TYPE A POTATO TALC SILICON DIOXIDE POVIDONE K30 FERRIC OXIDE RED POLYVINYL ALCOHOL, UNSPECIFIED POLYETHYLENE GLYCOL, UNSPECIFIED G;2
Text on the package panel: Physicians Care Ibuprofen Label Physicians Care® 90015 Ibuprofen Pain Reliever/ Fever Reducer (NSAID) Pull To Open This Package for Households without Young Children. Coated Tablets Tamper-Evident Packets of 2 Tablets Do not use if packet is open or torn. Pill color may vary Ibuprofen 200 mg 100 Tablets (50 Packets, 2 tablets each) 90015 Ibuprofen Granules Label
What it is for
Purpose Pain reliever/fever reducer
Key warnings
Warnings Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: ■ hives ■ skin reddening ■ asthma (wheezing) ■ facial swelling ■ rash ■ shock ■ 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 …
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 0924-0076. Recalls are listed in FDA enforcement reports from 2004 onward.
Show as table
| Item | Value (reports) |
|---|---|
| Drug ineffective | 15,939 |
| Pain | 15,218 |
| Fatigue | 14,700 |
| Nausea | 13,731 |
| Headache | 12,253 |
| Arthralgia | 11,066 |
| Dyspnoea | 10,670 |
| Vomiting | 10,129 |
| Diarrhoea | 9,841 |
| Rash | 9,151 |
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 (6)
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 9, 2026. The FDA notes this data should not be relied on alone for medical decisions. Not medical advice.