0.9% Sodium Chloride Injection, Solution
Product Images NDC 51662-1359

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

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for 0.9% Sodium Chloride (NDC 51662-1359). 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
FDA Label Image

How Supplied (How Supplied)

How Supplied (How Supplied)
A data table listing various units of sale and concentrations for 0.9% Sodium Chloride injection solution. It includes multiple NDC codes for single-dose cartridges and plastic fliptop vials with varying volumes from 2 mL to 50 mL and different packaging configurations, such as tubs and trays of 25 or 50 units.*
FDA Label Image
FDA Label Image

Serialized 50ml Vial (Serialized Vial)

Serialized 50ml Vial (Serialized Vial)
0.9% Sodium Chloride Injection, USP 50 mL single-dose vial with a green cap. The label indicates it is for use as a sterile diluent, distributed by HF Acquisition Co LLC, and manufactured for Hospira, Inc., Lake Forest, IL.*
FDA Label Image

Vial Label (Vial Label)

Vial Label (Vial Label)
Label for 0.9% Sodium Chloride Injection, USP 50 mL single-dose vial, preservative-free, for use as a sterile diluent. Contains 9 mg/mL sodium chloride, possibly with HCl and/or NaOH for pH adjustment. Manufactured by Hospira, Inc., Lake Forest, IL, labeled as Rx only with NDC 0409-4888-06.*

* 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.