Representative Image Of Figure 1-3 (Image 01)
Sodium Chloride Injection
Product Images NDC 0338-9151
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 Sodium Chloride (NDC 0338-9151). 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.
Pictures 4 (6.jpg)
List 7 8 9 (Image 03)
This is a set of instructions for administering medication using an administration set. The instructions suggest removing the port protector, attaching the administration set, and hanging the container on an LV pole. The user must also prime the set and ensure the vial is empty of drug and solution. It warns against using the medication in series connections and advises the user to administer the medication per the specified directions and within the specified time for drug stability.*
Representative Container Label 0338-9159-30 (Image 05)
Representative Container Label 0338-9151-30 (Image 06)
This is a label from a medical product. It contains instructions to "break seal and mix before use". The product has a unique identification code NDC 0338-9151-30 and contains 0.9% Sodium Chloride. The product is meant for intravenous use and the pharmacist should be consulted for additive compatibility. It should be stored at room temperature and protected from excessive heat. The product is made by Baxter Healthcare Corporation in Ireland. The expiration date is not available.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
