0.9% Sodium Chloride
Product Images NDC 51662-1260

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 0.9% Sodium Chloride (NDC 51662-1260). 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.

Product Images & Figures Index

FDA Label Image

Serialized Bag (1260 1 Serialized Bag And Label)

Serialized Bag (1260 1 Serialized Bag And Label)
Packaged 500 mL intravenous bag of 0.9% Sodium Chloride Injection, USP from HF Acquisition Co LLC, DBA HealthFirst. The clear bag contains sterile saline solution for injection with visible manufacturer branding and lot/expiration details printed on the front. The label states it is Rx only and lists the NDC 0409-7983-35.*
FDA Label Image

500 mL Bag (500 mL Bag)

500 mL Bag (500 mL Bag)
Label for 0.9% Sodium Chloride Injection, USP in a 500 mL size. The label includes ingredient details, usage instructions specifying intravenous use, and manufacturer information for Hospira, Inc. The label also shows NDC code 0409-7983-55, recycling symbols, and indicates the product is Rx only.*
FDA Label Image
Logo (How Supplied Logo)
FDA Label Image

How Supplied Tabel (How Supplied)

How Supplied Tabel (How Supplied)
A data table listing various NDC numbers for 0.45% and 0.9% Sodium Chloride Injection, USP products. The table includes product names and corresponding container sizes in milliliters, ranging from 25 mL to 1000 mL.*

* 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.