Cromolyn Sodium
Product Images NDC 17478-291

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Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Cromolyn Sodium (NDC 17478-291). 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.

Product Images & Figures Index

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This is a 10mL sterile ophthalmic solution containing Cromolyn Sodium 40mg/mL (4%) as the active ingredient, with Edetate Disodium (0.1%) and Water for Injection as the inactive ingredients. The solution should be stored between 20° to 25°C (68° to 77°F), and must be protected from light. The recommended dosage for ophthalmic use is 1-2 drops in each eye, 4 to 6 times a day at regular intervals, as indicated in the package insert. The solution is preserved with Benzalkonium Chloride (0.01%). This solution is for ophthalmic use only.*
FDA Label Image

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Cromolyn Sodium Ophthalmic Solution, USP is a prescription medicine used for ophthalmic purposes only. It is manufactured by Akorn, Inc. and contains 40mg (4%) Cromolyn Sodium, 0.1% Edetate Disodium Sodium and water for injection. Additionally, it contains 0.01% Benzalkonium Chloride as a preservative. The recommended dosage is one or two drops applied in each eye 4 to 6 times per day, as prescribed by a doctor. Patients must not touch the dropper tip to any surface and store the bottle in its original carton at tightly closed conditions, away from light and children. The package contains 10mL Cromolyn Sodium Ophthalmic Solution, USP. Detailed dosage information is available in the package insert.*

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