Elliotts B Injection
Product Images NDC 55792-007

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Elliotts B (NDC 55792-007). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lukare Medical, Llc, 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

Ampule Labeling (Ampule)

Label for Elliotts B Solution sterile intrathecal injection, 10 mL single-use ampule. Contains sodium chloride 7.3 mg, sodium bicarbonate 1.9 mg, hydrous dextrose 0.8 mg, magnesium sulfate 0.3 mg, potassium chloride 0.3 mg, calcium chloride 0.2 mg, sodium phosphate 0.2 mg, and water for injection 1.0 mL per mL. Distributed by Lukare Medical, LLC.*

FDA Label Image

Box Labeling (Carton)

The packaging label for Elliotts B Solution, a buffered intrathecal electrolyte/dextrose injection provided in ten 10 mL single-use ampules. The label lists active ingredients with amounts per milliliter including sodium chloride 7.3 mg, sodium bicarbonate 1.9 mg, dextrose 0.8 mg, magnesium sulfate 0.3 mg, potassium chloride 0.3 mg, calcium chloride 0.2 mg, and sodium phosphate 0.2 mg, with water for injection 1.0 mL. Distributed by Lukare Medical, LLC, this sterile prescription injection is for intrathecal use only.*

* 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.