Isotretinoin Capsule, Liquid Filled
Product Images NDC 68308-575

3 FDA label images from Mayne Pharma · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Isotretinoin (NDC 68308-575). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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

Product Images & Figures Index

FDA Label Image

Chemical Structure (Isotretinoin 01)

Chemical Structure (Isotretinoin 01)
Chemical structure diagram of the active ingredient isotretinoin, showing its molecular framework including rings and multiple double bonds, and a carboxylic acid functional group at one end.*
FDA Label Image

Figure 1 (Isotretinoin 02)

Figure 1 (Isotretinoin 02)
A line graph depicting mean lesion count over time (from baseline to week 20) during analysis visits for Isotretinoin capsules compared to Isotretinoin. The y-axis shows mean lesion count and the x-axis shows analysis visits at baseline, weeks 4, 8, 12, 16, and 20, with lesion counts declining over the study period for both groups.*
FDA Label Image

Principal Display Panel (40 mg Capsule Prescription Pack Carton)

Principal Display Panel (40 mg Capsule Prescription Pack Carton)
Packaging label for Isotretinoin Capsules, USP 40 mg, liquid-filled oral capsules. The label indicates 30 capsules (3 x 10 prescription packs) per package. Prominent warnings about birth defects and pregnancy prevention are displayed. The labeler is Mayne Pharma, with storage instructions and pharmacist dispensing guidance noted. NDC 68308-575-30 appears on the label.*

* 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.