Ibuprofen Mini (Ibuprofen Mini 200 mg)
TARGET CORPORATION · capsule, liquid filled · NDC 11673-683
Ibuprofen Mini is an over-the-counter medicine made available by TARGET CORPORATION, on the U.S. market since December 2021. It is marketed under an FDA approval (ANDA ANDA079205), 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 Jan 3, 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: Ibuprofen Mini Ibuprofen Mini 200 mg PROPYLENE GLYCOL FD&C GREEN NO. 3 GELATIN WATER SORBITAN MONOOLEATE POLYETHYLENE GLYCOL, UNSPECIFIED POTASSIUM HYDROXIDE FERROUS OXIDE MEDIUM-CHAIN TRIGLYCERIDES AMMONIA IBUPROFEN IBUPROFEN SORBITOL SHELLAC 62
Text on the package panel: 700T-TG-80s-label 700T-TG-300s-label 700T-TG-160s-label 700T-TG-160s-ifc 700T-TG-80s-ifc
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 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…
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 11673-683. Recalls are listed in FDA enforcement reports from 2004 onward.
Official listing
Active ingredients
Packages (3)
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.