Sodium Chloride Injection, Solution
Product Images NDC 0338-9657

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 0338-9657). 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

Representative Container Label Ndc 0338-9543-01 (Image 01)

Representative Container Label Ndc 0338-9543-01 (Image 01)
This is a description of a pharmaceutical product, 0.9% Sodium Chloride Injection USP. Each 100 mL of the solution contains 900 mg of Sodium Chloride USP with a mEg/L Sodium and Chloride concentration of 154. It comes in a single-dose container with an osmolarity of 308 mOsmL. The product must be used intravenously as directed by a physician using aseptic technique and must not be stored when leaks are found in the inner bags. The product must not be used in series connections and should only be used when the solution is clear. It should be stored in moistur barrier overwrap at room temperature. The text also contains a lot and expiry number which could indicate its manufacturing and expiry date.*
FDA Label Image

Sodium Chloride Representative Carton Label (Image 2)

Sodium Chloride Representative Carton Label (Image 2)
This is a description of a product named UE1324. It comes in 10x1000mL packaging totaling 11.5 kg. The product is 0.9% Sodium Chloride Injection with a formula of sodium chloride 3 cents and water for injection. It has an osmolarity of 308 mOsm/L and approximated mmol per 1000 mL of sodium 154 and chloride 154. The PH is 5.0 (4.5 – 7.0). It is for IV administration and users are advised to read the package insert before use. The product should be kept out of the reach and sight of children and users should not connect partially used drugs. The product is made in Spain by Baxter Healthcare Corporation with Lot:X0 and Part i P222E644. There is a barcode on the package. The expiry dates and batch numbers are not available.*

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