Gentak
Product Images NDC 67296-0114

View Photos of 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 Gentak (NDC 67296-0114). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Structural Formula (Gen03 0005 01)

Structural Formula (Gen03 0005 01)
Chemical structure diagram showing the molecular structure of Gentamicin, the active ingredient in Gentak. The image presents atomic connections and elements typical for this antibiotic compound, including carbon, hydrogen, oxygen, nitrogen, and phosphate groups.*
FDA Label Image

Principal Display Panel Text For Container Label (Gen03 0005 02)

Principal Display Panel Text For Container Label (Gen03 0005 02)
Label for Gentak ophthalmic ointment, 0.3% gentamicin sulfate equivalent to 3 mg gentamicin per gram, in a 3.5 g tube. The label states it is sterile, prescription only, and manufactured by Akorn, Inc. The ointment base contains white petrolatum and mineral oil.*
FDA Label Image

Principal Display Panel Text For Carton Label (Gen03 0005 03)

Principal Display Panel Text For Carton Label (Gen03 0005 03)
Packaging label for Gentak 0.3% ophthalmic ointment by Redpharm Drug, labeled as Gentamicin Sulfate Ophthalmic Ointment USP. The tube contains 3.5 g (1/8 oz.) of sterile ointment. The label includes storage instructions, dosage directions, preservatives listed, and manufacturer Akorn, Inc., Lake Forest, IL. NDC 17478-284-35 is printed 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.