Redicare Ibuprofen 200mg (Ibuprofen 200mg)
Redicare LLC · tablet · NDC 71105-365
Redicare Ibuprofen 200mg is an over-the-counter medicine made available by Redicare LLC, on the U.S. market since February 2025. 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 Mar 4, 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: Redicare Ibuprofen 200mg Ibuprofen 200mg STEARIC ACID SILICON DIOXIDE SODIUM STARCH GLYCOLATE TYPE A POTATO FERRIC OXIDE RED POLYETHYLENE GLYCOL 4000 IBUPROFEN IBUPROFEN STARCH, CORN POVIDONE K30 TITANIUM DIOXIDE TALC Reddish Brown G;2
Text on the package panel: Box Box
What it is for
Purpose fever reducer *nonsteroidal anti-inflammatory drug
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 a nonsteroidal anti-inflammatory drug (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 o…
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 71105-365. Recalls are listed in FDA enforcement reports from 2004 onward.
Show as table
| Item | Value (reports) |
|---|---|
| Drug ineffective | 15,937 |
| Pain | 15,214 |
| Fatigue | 14,701 |
| Nausea | 13,731 |
| Headache | 12,255 |
| Arthralgia | 11,065 |
| Dyspnoea | 10,667 |
| Vomiting | 10,129 |
| Diarrhoea | 9,838 |
| Rash | 9,154 |
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 10, 2026. The FDA notes this data should not be relied on alone for medical decisions. Not medical advice.