Imiquimod Cream
Product Images NDC 68682-272

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Imiquimod (NDC 68682-272). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Oceanside Pharmacueticals, 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

Image 01

Image 01
A line graph showing cumulative complete clearance over weeks for Imiquimod Cream 3.75% compared to Vehicle. The x-axis represents time in weeks from 0 to 16, and the y-axis represents the cumulative complete clearance ranging from 0 to 1. The Imiquimod Cream line shows an increasing trend higher than the Vehicle throughout the period.*
FDA Label Image

Image 02

Image 02
An instructional illustration showing a hand holding and pressing the top of a small tube or container, likely demonstrating how to dispense or apply a topical cream. No text or branding is visible.*
FDA Label Image

Image 03

Image 03
Imiquimod Cream 3.75% pump label from Oceanside Pharmaceuticals. The label states it is for topical use only, not for ophthalmic, oral, or intravaginal use, and that the 7.5 g net weight cream delivers no fewer than 28 full actuations. Storage instructions specify to store upright and avoid freezing. The label includes the NDC 68682-272-75 and lists inactive ingredients. The background color is a soft blue gradient with branding logos at the bottom.*
FDA Label Image

Chemical Structure (Zyclara 01)

Chemical Structure (Zyclara 01)
Chemical structure of imiquimod showing its molecular arrangement, including an amino group, fused rings, and an isobutyl side chain.*

* 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.