Sodium Chloride
Product Images NDC 17478-622

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 17478-622). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Akorn, 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

Sod06 0004 01

Label for Sodium Chloride Ophthalmic Ointment USP 5%, a hypertonicity eye ointment. The label notes it is sterile and for ophthalmic use only. It provides the net weight of 3.5 g (1/8 oz) and includes active and inactive ingredients. Storage instructions and warnings such as "Do not use if bottom ridge of tube cap is exposed" are visible. The product is manufactured by Akorn, Inc., Lake Forest, IL 60045.*

FDA Label Image

Sod06 0004 02

Sodium Chloride Ophthalmic Ointment USP, 5% by Akorn is shown in packaging carton artwork. The product contains 3.5 g (1/8 oz.) of ointment for ophthalmic use only. The label indicates it is a hypertonicity eye ointment with inactive ingredients listed including mineral oil, modified lanolin, water for injection, and white petrolatum. The Drug Facts panel provides usage directions, warnings, and storage conditions on the carton.*

* 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.