Sulfamethoxazole And Trimethoprim Suspension
Product Images NDC 81033-012

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sulfamethoxazole And Trimethoprim (NDC 81033-012). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kesin Pharma, 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
FDA Label Image

Sulfamethoxazole And Trimethoprim 800mg/160mg Per 20ml Carton Label (Sulfa Trim Smx 20 mL Carton Label)

Sulfamethoxazole And Trimethoprim 800mg/160mg Per 20ml Carton Label (Sulfa Trim   Smx 20 mL Carton Label)
Label for Sulfamethoxazole and Trimethoprim Oral Suspension, USP 800mg/160mg per 20mL, a prescription human drug. The label shows packaging and distribution by Kesin Pharma Corporation, Oldsmar, FL, and indicates 40 unit dose cups of 20mL each. Storage instructions specify 68°F to 77°F (20°C to 25°C). The label is marked for institutional use only.*
FDA Label Image

Sulfamethoxazole Chemical Structure (Sulfamethoxazole Chemical Structure)

Sulfamethoxazole Chemical Structure (Sulfamethoxazole Chemical Structure)
Chemical structure of the active ingredient shown, depicting a molecular diagram with labeled atomic groups and bonds.*
FDA Label Image

Trimethoprim Chemical Structure (Trimethoprim Chemical Structure)

Trimethoprim Chemical Structure (Trimethoprim Chemical Structure)
Chemical structure of Sulfamethoxazole and Trimethoprim, showing the molecular arrangement of the two active ingredients typically found in the oral suspension form labeled by Kesin Pharma.*

* 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.