0.9% Sodium Chloride Injection, Solution
Product Images NDC 51662-1520

3 FDA label images from Hf Acquisition Co Llc, Dba Healthfirst · 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 0.9% Sodium Chloride (NDC 51662-1520). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Bag Label (Bag Label)

Bag Label (Bag Label)
Label for 0.9% Sodium Chloride Injection, USP in a 100 mL single-dose container. The label details the active ingredient strength as 900 mg per 100 mL, indicates intravenous use, and includes the manufacturer ICU Medical. It notes the solution is sterile, nonpyrogenic, and free of latex, with a caution about additives and usage instructions.*
FDA Label Image

How Supplied (How Supplied)

How Supplied (How Supplied)
A data table listing various NDC numbers, product names, and container sizes for Sodium Chloride Injection, USP in concentrations of 0.45% and 0.9%. Container sizes range from 25 mL to 1000 mL for different NDC-coded products, showing multiple entries for each size and concentration variant.*
FDA Label Image

Serialized Label (Serialized Label)

Serialized Label (Serialized Label)
0.9% Sodium Chloride Injection, USP 100 mL intravenous solution in a silver foil pouch. The label instructs to tear at the notch to open. Barcode and NDC 0990-7984-23 are visible. Distributed by HF Acquisition Co., LLC in Mukilteo, WA. Manufactured by ICU Medical, Inc., Lake Forest, Illinois, 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.