Uline Eyewash Solution
Product Images NDC 69790-010

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Uline Eyewash (NDC 69790-010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Uline., 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

Label (52195 Reva Fda Uline)

Label (52195 Reva Fda Uline)
This is a description of an ophthalmic solution for eyewash, consisting mainly of Purified Water at 98.3% for cleansing the eyes to relieve irritation and burning by removing loose foreign material. The product is intended for single-use and is sterile. Instructions include flushing the affected eye as needed and discarding the solution after one use. The solution should not be used if there are open wounds near the eyes or if the solution changes color or becomes cloudy. The inactive ingredients include boric acid, sodium borate, and sodium chloride. The product is distributed by ULINE, Inc., and manufactured in Canada. It is important to keep the solution out of reach of children and seek medical help if swallowed. The product's contact information is provided for questions or concerns.*

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