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

Sodium Chloride Ophthalmic Ointment USP is a hypertonicity eye ointment with a net weight of 3.5g, which is used for the temporary relief of corneal edema. This ointment is meant for ophthalmic use only and should be applied every 3 to 4 hours, or as directed by a doctor. Its active ingredient is Sodium Chloride 5% (50 mg/g) and inactives include Mineral Oil, Modified Lanolin, Water for Injection, and White Petrolatum. It should be stored at 20° to 25°C (68° to 77°F) and Keep Tightly Closed. The Lot Number and Expiration Date can be found on the crimp.*

FDA Label Image

Sod06 0004 02

This is a Drug Facts label for an ophthalmic ointment. The active ingredient is Sodium Chloride 5%, which is a hypertonicity agent used for temporary relief of corneal edema. The ointment is only for ophthalmic use, and it should not be used unless under the advice and supervision of a doctor. It may cause temporary burning and irritation upon application into the eye. The ointment should be stored at 20°to 25°C and away from heat as well as protected from freezing. In case of eye pain, changes in vision, continued redness, or irritation of the eye, stop the use and contact a doctor. For almost any questions, call 1-800-932-5676.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.