Plasma-lyte A Injection, Solution
Product Images NDC 0338-0221

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Plasma-lyte A (NDC 0338-0221). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Carton Label (Image 01)

This text panel provides printing instructions for a Plasma-Lyte A injection solution container. It includes placeholders for expiration date, lot number, primary and secondary bar codes, and notes on date format and barcode encoding for a 14-1000 mL Viaflex container.*

FDA Label Image

Container Label (Image 02)

Label for Plasma-Lyte A Injection pH 7.4, a sterile intravenous injection solution with multiple electrolytes including sodium chloride, sodium gluconate, sodium acetate, potassium chloride, and magnesium chloride. The label specifies a 1000 mL volume and details electrolyte concentrations per 100 mL. It also includes usage instructions, storage conditions, and manufacturer information from Baxter Healthcare Corporation, Deerfield, IL, USA.*

* 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.