Sodium Chloride
Product Images NDC 51662-1318

4 FDA label images from Hf Acquisition Co Llc, Dba Healthfirst · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 51662-1318). 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

Serialized Labeling (51662 1318 1 Resized Serialized Labeling)

Serialized Labeling (51662 1318 1 Resized Serialized Labeling)
Packaging label for SODIUM CHLORIDE 0.9% Injection, USP in a 100 mL sterile packet. The label includes instructions to tear at the notch to open, a barcode, and a note that it is for Rx only. Distributed by HF Acquisition Co LLC, DBA HealthFirst, the package also shows a secondary label with lot and expiration information.*
FDA Label Image

Bag (Bag Label)

Bag (Bag Label)
Label of 0.9% Sodium Chloride Injection, USP, 100 mL single-dose container by Hospira, Inc. The label includes dosage and composition details, sterility and usage instructions, barcode, and manufacturer information (Hospira, Lake Forest, IL). It indicates the product is nonpyrogenic, intended for IV use, latex information, and contains DEHP.*
FDA Label Image

How Supplied (How Supplied)

How Supplied (How Supplied)
A data table listing multiple NDC numbers for Sodium Chloride injection solutions, USP in concentrations of 0.45% and 0.9%. The table includes various container sizes ranging from 25 mL to 1000 mL for each product variant, showing corresponding NDC codes.*
FDA Label Image

* 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.