Phenobarbital
Product Images NDC 17856-0502

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Phenobarbital (NDC 17856-0502). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Atlantic Biologicals Corp., 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

Image 1 (17856 0502 01 Phenobarbital)

Label for Phenobarbital oral solution 20 mg/5 mL by Atlantic Biologicals Corp. The label includes storage instructions to keep at 20°-25°C (68°-77°F), shake well before use, and alcohol content of 15%. The package contains 72 unit dose cups, each with 5 mL dosage. It also provides reorder contact information and batch details.*

FDA Label Image

Image 2 (17856 0502 02 Phenobarbital)

Phenobarbital oral solution 30 mg per 7.5 mL unit dose label from ATLANTIC BIOLOGICALS CORP. The label includes storage instructions at 20°-25°C (68°-77°F), a warning to shake well, and notes 15% alcohol content. The package contains 72 unit dose cups, with a reorder phone number and packaging and distribution information also displayed.*

FDA Label Image

17856 0502 03

Packaging label for Phenobarbital Oral Solution, USP 20 mg/5 mL, by Atlantic Biologicals Corp. The label indicates storage instructions at 20°-25°C (68°-77°F) and notes alcohol content of 15%. The package quantity is 48 unit dose syringes, each with a 5 mL dosage. Packaging and distribution details include Unit Dose Solutions, Morrisville, NC, and Atlantic Biologicals Corp., Miami, FL.*

FDA Label Image

Chemical Structure (Phenobarbital 01)

Chemical structure diagram of phenobarbital showing its molecular rings, including the barbiturate core and attached ethyl and phenyl groups.*

* 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.