Bacteriostatic Sodium Chloride Injection
Product Images NDC 63323-924

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 Bacteriostatic Sodium Chloride (NDC 63323-924). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, Llc, 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

Logo (Bac0a 0000 01)

Logo (Bac0a 0000 01)
Bacteriostatic Sodium Chloride 9 mg/mL injection vial label from Fresenius Kabi USA, LLC. The label includes the product name, strength, and the company name with location in Lake Zurich, IL. The label is primarily blue and white with the Fresenius Kabi logo.*
FDA Label Image

924830-vial (Bac0a 0000 02)

924830-vial (Bac0a 0000 02)
Label for Bacteriostatic Sodium Chloride Injection, USP 0.9%, 30 mL multiple dose vial. The label states it is not for use in newborns and is for drug diluent use only, not for inhalation. The product is identified by NDC 63323-924-03 and made by Fresenius Kabi USA, LLC.*
FDA Label Image

Package Label – Principal Display (Bacteriostatic Sodium Chloride 30 mL Multiple Dose Vial Tray Label)

Package Label – Principal Display (Bacteriostatic Sodium Chloride 30 mL Multiple Dose Vial Tray Label)
Label for Bacteriostatic Sodium Chloride Injection USP 0.9%, 30 mL multiple dose vial. Contains 9 mg/mL sodium chloride with 0.9% benzyl alcohol as a preservative. Pack includes 25 vials. Sterile, nonpyrogenic formulation by Fresenius Kabi USA, LLC. Storage instructions and usual dosage reference included. Not for use in newborns or inhalation; for drug diluent use only.*

* 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.