Physicians Care Ibuprofen (Ibuprofen 200mg)

Acme United Corporation · tablet, coated · NDC 0924-0075

Listed in the FDA National Drug Code directory

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 ANDA075010), 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 STEARIC ACID TITANIUM DIOXIDE STARCH, CORN HYPROMELLOSES SILICON DIOXIDE FERRIC OXIDE RED LACTOSE CELLULOSE, MICROCRYSTALLINE POLYDEXTROSE POLYETHYLENE GLYCOL, UNSPECIFIED CARNAUBA WAX IBUPROFEN IBUPROFEN MAGNESIUM STEARATE SODIUM STARCH GLYCOLATE TYPE A POTATO 44;291

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 Ibuptofen 200mg 100 Tablets (50 packets, 2 tablets each) 90015 Jpeg

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.

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Recalls of this product

No FDA recalls are recorded for NDC 0924-0075. Recalls are listed in FDA enforcement reports from 2004 onward.

Most reported side effects for ibuprofen 200mgReports to the FDA Adverse Event Reporting System (FAERS), all products with this ingredient
Drug ineffective15,939 reports
Pain15,218 reports
Fatigue14,700 reports
Nausea13,731 reports
Headache12,253 reports
Arthralgia11,066 reports
Dyspnoea10,670 reports
Vomiting10,129 reports
Diarrhoea9,841 reports
Rash9,151 reports
Show as table
ItemValue (reports)
Drug ineffective15,939
Pain15,218
Fatigue14,700
Nausea13,731
Headache12,253
Arthralgia11,066
Dyspnoea10,670
Vomiting10,129
Diarrhoea9,841
Rash9,151

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

Brand
Physicians Care Ibuprofen
Generic name
Ibuprofen 200mg
Company
Acme United Corporation
Form
tablet, coated
Route
oral
Type
HUMAN OTC DRUG
Category
ANDA
Listing valid to
Dec 31, 2026
Product NDC
0924-0075

Active ingredients

Ibuprofen
200 mg/1

Packages (6)

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

0924-0075-00 2 tablet, coated in 1 packet (0924-0075-00)
0924-0075-01 50 packet in 1 carton (0924-0075-01) / 2 tablet, coated in 1 packet (0924-0075-00)
0924-0075-02 125 packet in 1 carton (0924-0075-02) / 2 tablet, coated in 1 packet
0924-0075-03 10 packet in 1 carton (0924-0075-03) / 2 tablet, coated in 1 packet (0924-0075-00)
0924-0075-04 6 packet in 1 carton (0924-0075-04) / 2 tablet, coated in 1 packet (0924-0075-00)
0924-0075-05 20 packet in 1 carton (0924-0075-05) / 2 tablet, coated in 1 packet (0924-0075-00)

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.