Ibuprofen Minis Capsule, Liquid Filled
Product Images NDC 30142-743

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Ibuprofen Minis (NDC 30142-743). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by The Kroger Co., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Solubilized Ibuprofen Equal To 200 mg Ibuprofen (nsaid)* (present As The Free Acid And Potassium Salt) *nonsteroidal Anti-inflammatory Drug (Ibuprofen 200 mg Mini Softgels Pur 1)

Solubilized Ibuprofen Equal To 200 mg Ibuprofen (nsaid)* (present As The Free Acid And Potassium Salt) *nonsteroidal Anti-inflammatory Drug (Ibuprofen 200 mg Mini Softgels Pur 1)
This is a drug facts sheet for Ibuprofen Capsules 200mg, a pain reliever and fever reducer. The active ingredient in each capsule is Solubilized Buprofen equal to 200mg Ibuprofen, a nonsteroidal anti-inflammatory drug. The drug is used for pain relief but if you have heart problems, high blood pressure, kidney disease or asthma, had a stroke or are under a doctor's care for any serious condition, you should speak to a doctor or pharmacist before use. The drug may cause severe allergic reactions, stomach bleeding or be harmful during pregnancy. One capsule should be taken every 4-6 hours while symptoms persist, but not more than 6 capsules in 24 hours. Children under the age of 12 should ask a doctor. The product should be kept out of reach of children, and the warnings and directions should be read before use. The product is comparable to Advil Liqui-Gels Minis.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.