Motrin Ib Tablet, Film Coated
Product Images NDC 85237-1947

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Motrin Ib (NDC 85237-1947). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Select Consumer Group Llc, 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

1 (2611947022 Motrin Ib 1947 1)

Motrin IB Ibuprofen Tablets USP 200 mg film-coated tablets packaging label displaying a 2-coat caplets single-pack blister card. The front shows the Motrin IB brand name, ibuprofen as the active ingredient, and highlights pain reliever/fever reducer (NSAID). The back includes detailed drug facts, usage warnings, directions, inactive ingredients, and distributor information by Johnson & Johnson Consumer Inc. and Select Corporation.*

FDA Label Image

2 (2621947033 Motrin Ib 1947 2)

Motrin IB 200 mg coated caplets multi-pack packaging label. The front shows the brand name Motrin IB, the active ingredient ibuprofen 200 mg, and states pain reliever/fever reducer (NSAID). The package contains four coated caplets. The back panel includes detailed Drug Facts, warnings, directions, and inactive ingredients. The product is labeled for oral use and distributed by Johnson & Johnson Consumer Inc., repackaged by Select Corporation.*

FDA Label Image

7 (2631947034 Motrin 1947 7)

Motrin IB Ibuprofen Tablets USP, 200 mg film coated tablets in a 6 coated caplets multi-pack. The front displays the brand name, active ingredient, and strength with an illustration of two orange caplets marked 'MOT'. The back includes detailed Drug Facts, warnings, usage directions, inactive ingredients, and distributor information by Select Consumer Group LLC.*

* 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.