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

View Photos of 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)
The text contains details about the unit of sale for different products. The products include Carpuject cartridges with Luer Lock for the Carpuject Syringe System, single-dose plastic flip-top vials, and single-dose Lifeshield PlnstREiptopals. The products are available in different sizes ranging from 2 mL to 50 mL with different package sizes such as tubs and trays. All products have 0.9% concentration.*
FDA Label Image
FDA Label Image

Serialized 50ml Vial (Serialized Vial)

Serialized 50ml Vial (Serialized Vial)
This is a label or packaging for an item called "50 mL Single-dose" with a manufacturer named "HOSplra". It is intended for use as a sterile solution. The location of manufacture or distribution is in the USA. No further information is available.*
FDA Label Image

Vial Label (Vial Label)

Vial Label (Vial Label)
This is a description for a pharmaceutical product. The product is a single-dose medication contained in a 50 mL container, and it is only available through a prescription (Rxonly). The medication is preservative-free and is used as a sterile diluent. Each mL of the medication contains 9mg of sodium chloride, and it may contain HCl and/or NaOH for pH adjustment. The medication is sterile and nonpyrogenic. The manufacturer is Hospira, Inc., located in Lake Forest, IL 60045, USA. The reference code for the product is RL-4494, and its National Drug Code (NDC) is 0409-4888-06.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.