0.9% Sodium Chloride Injection, Solution
Product Images NDC 51662-1517

View Photos of 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 51662-1517). 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 (0990 7983 02 Sodium Chloride Bag Label)

Bag Label (0990 7983 02 Sodium Chloride Bag Label)
This is a 0.9% Sodium Chloride Injection, USP with 250 mL in a single-dose container for intravenous use. Each 100 mL of the injection contains Sodium Chloride 900 mg electrolytes per 1000 mL: Sodium 154 mEq and Chloride 154 mEq. It is a sterile, nonpyrogenic solution that should be used only if the solution is clear, and the container is undamaged. Additives may be incompatible, thus consultation with a pharmacist is needed. This product contains DEHP and must not be used in series connections. The pH of the solution is 5.6 and has a calculated osmolality of 308 mOsmol/liter. The usual dosage is indicated in the insert.*
FDA Label Image

Hf Label (0990 7983 02 Sodium Chloride Hf Label)

FDA Label Image

How Supplied (How Supplied)

How Supplied (How Supplied)
This text seems to be a list of National Drug Codes (NDCs) for products containing either 0.45% or 0.9% Sodium Chloride Injection USP in varying quantities. The NDCs are a unique 10-digit identifier assigned to each medication listed under the Federal Food, Drug, and Cosmetic Act.*

* 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.