Sulfatrim
Product Images NDC 67296-1657

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sulfatrim (NDC 67296-1657). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

100 200ml Labels (67296 1657)

Two pharmaceutical labels for SULFATRIM Pediatric oral suspension by RedPharm Drug, Inc. Each label displays the active ingredients sulfamethoxazole and trimethoprim, strength 200 mg/40 mg per 5 mL, and directions to shake well. One label indicates a 200 mL bottle, the other a 100 mL bottle. Both include storage instructions, lot numbers (masked), expiration dates (masked), alcohol content at 0.5%, and barcodes.*

FDA Label Image

Chemical Structure (Sulfatrim 01)

Chemical structure of SULFATRIM's active ingredient, showing the molecular arrangement including an amino group, a sulfonamide group attached to a benzene ring, and an oxadiazole ring with a methyl substituent.*

FDA Label Image

Chemical Structure (Sulfatrim 02)

Chemical structure diagram showing the molecular formula of the active ingredient in SULFATRIM by RedPharm Drug, Inc. The illustration includes ring structures and functional groups characteristic of the compound.*

FDA Label Image

Principal Display Panel (473 mL Bottle Label)

Label for Sulfatrim Pediatric Suspension, an oral suspension containing sulfamethoxazole 200 mg and trimethoprim 40 mg per 5 mL, cherry flavor. The 16 fl oz (473 mL) bottle is manufactured for Pharmaceutical Associates, Inc., Greenville, SC. Label includes storage instructions, dosage advisory, and a warning to keep out of reach of children.*

* 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.