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

3 FDA label images from Bausch & Lomb Incoporated · Packaging, Regulatory Labels, and Product Appearance

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)

Sulfacetamide Sodium (structural Formula) (4dac0038 71cb 488e 9dd8 670fcf7b2073 01)
Chemical structure diagram of Sulfacetamide Sodium showing its molecular components, including the amino group, sodium sulfonamide moiety, and hydrate form with water (H2O).*
FDA Label Image

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

Prednisolone Sodium Phosphate (structural Formula) (4dac0038 71cb 488e 9dd8 670fcf7b2073 02)
Chemical structure diagram of the active ingredient prednisolone sodium phosphate showing its molecular framework including hydroxyl, carbonyl, and phosphate groups associated with the corticosteroid structure.*
FDA Label Image

Carton (Carton)

Carton (Carton)
Box packaging label for Sulfacetamide Sodium and Prednisolone Sodium Phosphate Ophthalmic Solution 10%/0.23% sterile drops, 5 mL, from Bausch & Lomb Incorporated. The label displays active and inactive ingredients, storage instructions, dosage directions, and warnings including 'For Ophthalmic Use Only' and 'Rx only'. The packaging includes barcodes on both flap and side panels.*

* 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.