Imiquimod Cream
Product Images NDC 51672-4174

5 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Imiquimod (NDC 51672-4174). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, Inc., 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

Chemical Structure (Imiquimod 01)

Chemical Structure (Imiquimod 01)
Chemical structure of Imiquimod, showing its molecular arrangement with nitrogen and carbon atoms including a substituted imidazoquinoline framework.*
FDA Label Image

Figure 1 (Imiquimod 02)

Figure 1 (Imiquimod 02)
A line graph showing cumulative complete clearance over time (weeks) comparing Imiquimod 3.75% cream to vehicle. The graph illustrates an increasing clearance trend for Imiquimod 3.75% over 16 weeks, while the vehicle shows a relatively flat clearance rate.*
FDA Label Image

Principal Display Panel (28 Packet Carton)

Principal Display Panel (28 Packet Carton)
An instructional line drawing showing a hand holding a small tube, likely demonstrating how to hold or apply a topical cream product. No text or product branding is visible on the tube.*
FDA Label Image

Imiquimod 04

Imiquimod 04
Imiquimod Cream USP 3.75% packaging label for topical use, containing 28 single-use packets each with 0.25 g (net 7 g per box). Label includes NDC 51672-4174-6, manufacturer Taro Pharmaceutical Industries Ltd., and distributor Taro Pharmaceuticals U.S.A., Inc. Warnings emphasize keeping medication out of children's reach, and it is marked Rx only.*
FDA Label Image

Imiquimod 05

Imiquimod 05
Packaging label for Imiquimod Cream USP 3.75% Pump, 7.5 g, a topical prescription drug by Sun Pharmaceutical Industries, Inc. The label includes storage instructions, active ingredient content, warnings against ophthalmic, oral, or intravaginal use, and manufacturer details. The product is distributed by Taro Pharmaceuticals U.S.A., with instructions to store upright and keep out of children's reach.*

* 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.