Sodium Chloride Injection, Solution
Product Images NDC 0990-7983

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 0990-7983). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Icu Medical 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

Principal Display Panel (50 mL Bag Label)

Label for Sodium Chloride Injection, USP 0.45%, 450 mg/100 mL in a 50 mL container. The label states that each 100 mL contains sodium chloride in water for injection, with specified electrolyte content and pH range. It includes usage and storage instructions, single-dose container designation, latex and recycling symbols, and lists ICU Medical Inc. as the labeler, located in Lake Forest, Illinois.*

FDA Label Image

Principal Display Panel (250 mL Bag Label)

Sodium Chloride 0.9% Injection USP label for a 250 mL single-dose container by ICU Medical Inc. The label states the solution contains 900 mg sodium chloride per 100 mL and is for intravenous use. It includes usage warnings about additives and container conditions, with official markings such as Rx only, DEHP content, latex-free symbol, and lot code IM-4450.*

FDA Label Image

Principal Display Panel (25 mL Bag Label)

Label for Sodium Chloride Injection USP 900 mg/100 mL in a 25 mL vial. The label states the active ingredient's concentration, electrolytes content, pH range (6.0), usage instructions for intravenous use, sterility, and packaging details. It is manufactured by ICU Medical Inc., Lake Forest, Illinois.*

FDA Label Image

Principal Display Panel (500 mL Bag Label)

Label of 0.45% Sodium Chloride Injection, USP, 450 mg/100 mL in 500 mL single-dose container by ICU Medical Inc. It is sterile, nonpyrogenic, for intravenous use only, and contains latex and DEHP. The label includes electrolyte concentrations, pH range, and usage cautions.*

* 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.