Atovaquone Suspension
Product Images NDC 51407-642

View Photos of 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 Atovaquone (NDC 51407-642). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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

51407-642-87cb.jpg (51407 642 87cb)

51407-642-87cb.jpg (51407 642 87cb)
Atovaquone Oral Suspension, USP 750 mg/5 mL carton label by Golden State Medical Supply, Inc. The packaging includes the NDC number 51407-642-87, dosage strength, and instructions for storage and handling. The carton also displays the GSMS incorporated logo and directions to shake gently before use, with warnings about tamper-evident seals and freezing.*
FDA Label Image

51407-642-87ol.jpg (51407 642 87ol)

51407-642-87ol.jpg (51407 642 87ol)
Atovaquone 750 mg/5 mL oral suspension label displaying the product name, strength, and dosage form. The label includes the NDC number 51407-642, a 210 mL bottle size, and mentions it is Rx only. It warns to shake gently before use, not to freeze, and to keep out of reach of children. Manufactured by CoreRx, Inc. and marketed by GSMS, Incorporated in Camarillo, CA. The label also includes storage temperature instructions and a tamper-evident seal warning.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of Atovaquone, showing a naphthoquinone core with a hydroxyl group and a chlorophenylcyclohexyl substituent, corresponding to the active ingredient Atovaquone.*

* 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.