Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percent Ointment
Product Images NDC 59390-184

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percent (NDC 59390-184). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Altaire 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.

FDA Label Image

Compare To The Active Ingredient In Muro128®*isolutions™activeyes®altachloresodium Chloride Hypertonicity Ophthalmic Ointment 5%•for Temporary Relief Of Corneal Edemasterile Net Wt 3.5g (1/8 Oz)*this Product Is Not Manufactured Or Distributed By Bausch & Lomb, Inc., Owner Of The Registered Trademark Muro128® (Altachlore Sodium Chloride Hypertonicity Ophthalmi 01)

Compare To The Active Ingredient In Muro128®*isolutions™activeyes®altachloresodium Chloride Hypertonicity Ophthalmic Ointment 5%•for Temporary Relief Of Corneal Edemasterile Net Wt 3.5g (1/8 Oz)*this Product Is Not Manufactured Or Distributed By Bausch & Lomb, Inc., Owner Of The Registered Trademark Muro128® (Altachlore Sodium Chloride Hypertonicity Ophthalmi 01)
Packaging label for Altachlore Sodium Chloride Hypertonicity Ophthalmic Ointment 5%, containing 50 mg/g sodium chloride. The label shows that it is an ophthalmic ointment for temporary relief of corneal edema, with a net weight of 3.5 grams (1/8 oz), sterile. The labeler is Altaire Pharmaceuticals Inc. The label also includes usage instructions, warnings, inactive ingredients, and a barcode.*

* 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.