Zinc Oxide 20%
Product Images NDC 54162-040

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zinc Oxide 20% (NDC 54162-040). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Geritrex 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

28g Label (Geritrex Zincoxide 28g 5416204028)

The image shows the packaging label for Zinc Oxide 20% Ointment by GERITREX LLC. The label indicates the product is a skin protectant for external use only, with a net weight of 1 ounce (28 grams). It includes the Drug Facts panel, warnings, directions, other information, and active ingredient details. The label also displays the NDC number 54162-040-28 and contact information for the distributor, GERITREX LLC.*

FDA Label Image

454g Label (Geritrex Zincoxide 454g 5416204016)

Label for Zinc Oxide 20% Ointment, a skin protectant by Geritrex LLC. The ointment is for external use only, with a net weight of 1 lb (454 g). The label includes Drug Facts such as active ingredient (Zinc Oxide 20%), uses, warnings, directions for use, storage information (controlled room temperature 20-25°C), inactive ingredients (mineral oil and white petrolatum), and distributor contact details for Geritrex LLC in Middletown, NY.*

FDA Label Image

56g Label (Geritrex Zincoxide 56g 5416204056)

Label for Zinc Oxide 20% Ointment by Geritrex LLC, a skin protectant for external use. The net weight is 56 grams (2 oz). The label includes drug facts such as active ingredient, purpose, uses, warnings, directions, other information, and inactive ingredients mineral oil and white petrolatum. Distributed by Geritrex, LLC, with contact information provided.*

* 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.