Sulfacetamide Sodium And Prednisolone Sodium Phosphate Solution/ Drops
Product Images NDC 24208-317

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sulfacetamide Sodium And Prednisolone Sodium Phosphate (NDC 24208-317). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bausch & Lomb Incoporated, 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

Sulfacetamide Sodium (structural Formula) (4dac0038 71cb 488e 9dd8 670fcf7b2073 01)

FDA Label Image

Prednisolone Sodium Phosphate (structural Formula) (4dac0038 71cb 488e 9dd8 670fcf7b2073 02)

FDA Label Image

Carton (Carton)

This is a description for an ophthalmic solution containing Sulfacetamide Sodium and Prednisolone Sodium Phosphate. It is distributed by Bausch + Lomb and manufactured by Bausch & Lomb Incorporated. The solution is for ophthalmic use only and has Actives: Sufacetamide Sodium 100g, Prednisolone Sodiym Phosphate 2.5mg (equivalent to Prednisolone Phosphate 2.3mg). The Inactives include Poloxarmer 407, Boric Acid, Edetate Disodium, Purified Water. Hydrochloric acid and/or Sodium Hydroxide may be added to adjust the pH. The preservative added is Thimerosal 0.01%. The recommended dosage is two drops into the eye(s) every four hours. The storage temperature is between 15°C to 25°C (59°F to 77°F).*

* 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.