Phenobarbital Sodium Injection
Product Images NDC 42494-416

3 FDA label images from Cameron Pharmaceuticals · 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 Phenobarbital Sodium (NDC 42494-416). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cameron Pharmaceuticals, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Chemical Structure (Phenobarbital 01)

Chemical Structure (Phenobarbital 01)
Chemical structure of Phenobarbital Sodium, showing a barbiturate ring with sodium salt and attached ethyl and phenyl groups consistent with its molecular configuration.*
FDA Label Image

Principal Display Panel (130 mg/mL Vial Box Label)

Principal Display Panel (130 mg/mL Vial Box Label)
The label for Phenobarbital Sodium Injection USP, 130 mg/mL, by Cameron Pharmaceuticals. It indicates the product is for intramuscular or slow intravenous use, packaged as 25 vials of 1 mL each. Storage instructions specify controlled room temperature, and a caution warns against use if the solution is discolored or contains precipitate. The label includes the NDC code 42494-416-25.*
FDA Label Image

Principal Display Panel (65 mg/mL Vial Box Label)

Principal Display Panel (65 mg/mL Vial Box Label)
Label for Phenobarbital Sodium Injection, USP 65 mg/mL for intramuscular or slow intravenous use. Pack contains 25 vials of 1 mL each. Manufactured by Cameron Pharmaceuticals LLC. The label includes storage instructions and warning against use if discolored or containing precipitate.*

* 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.