Sodium Chloride Injection
Product Images NDC 0338-9662

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 0338-9662). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Assembly 1-6 (Image 01)

This document provides guidance for the reconstitution of medications from vials. It explains steps such as removing the vial cover, inspecting the adapter, pushing it down until it snaps in place, and verifying that the vial is fully seated. It also details the process for preparing liquid and powdered drug vials, including shaking to suspend the drug in the solution and ensuring complete dissolution without removing the drug vial.*

FDA Label Image

Assembly 7-9 (Image 02)

This text provides instructions for a medical procedure involving the removal of a port protector and attaching an administration set following specific directions. It also mentions using a particular administration set and warns against using it in series connections. Additionally, it instructs on administering medication as per given directions within a specified timeframe for drug stability.*

FDA Label Image

Representative Container Label 0338-9660-40 (Image 03)

This text provides information about a medical product called 0.9% Sodium Chloride Injection USP in a Mine-Bag Plus Single Dose Container. It includes directions to break the seal and mix before use and mentions that each 50 mL contains 450 mg of Sodium Chloride USP and 8 mEq of Sodium Chloride. It also advises to refer to prescribing information for additive compatibility and consult a pharmacist for intravenous use. The product is to be stored at room temperature, and it is manufactured by Baxter Healthcare Corporation in Ireland.*

FDA Label Image

Representative Carton Label 0338-9660-40 (Image 04)

This is a 0.9% Sodium Chloride Injection in a mini-bag plus container with a quantity of 40 bags containing 50 mL each. The product is manufactured by Baxter Healthcare Corporation in Ireland. The NDC number is 0338-9660-40. It must be stored at room temperature (25°C/77°F). The lot number is 88G88G88B8.*

FDA Label Image

Representative Container Label 0338-9662-35 (Image 05)

This text provides important details about a medical product, including instructions to break the seal and mix before use. It specifies the contents of the product as 0.9% Sodium Chloride Injection USP in a container called MINE-BAG Prus SeLe Dose ConTamer. Each 100 mL contains 900 mg of Sodium Chloride USP. The document also indicates the manufacturer as Baxter Healthcare Corporation in the USA, with production in Ireland. It recommends consulting a pharmacist for additive compatibility for intravenous use and to store at room temperature to avoid excessive heat. This product is for prescription use only.*

FDA Label Image

Representative Carton Label 0338-9662-35.jpg (Image 06)

This is information about a product with the code EZPB0043G, consisting of 35 units of 100 mL 0.9% Sodium Chloride Injection, USP. It is stored at room temperature (25°C/77°F) and manufactured by Baxter Healthcare Corporation in Ireland. The text also includes NDC and DC numbers for reference.*

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