Uline Eyewash Solution
Product Images NDC 65785-125

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Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Uline Eyewash (NDC 65785-125). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Niagara Pharmaceuticals Inc., 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)
Drug Facts panel for ULINE Eyewash Saline, 473 mL ophthalmic solution. Lists purified water 98.3% as active ingredient, use instructions for eye cleansing, warnings, directions, storage, and inactive ingredients including boric acid, sodium borate, and sodium chloride. Includes bilingual English and Spanish sections, manufacturer ULINE, Inc., and a contact phone number.*

* 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.