Sodium Chloride Injection
Product Images NDC 0338-0553

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 0338-0553). 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 Pictures 1, 2 And 3 (Image 01)

An instructional diagram illustrating steps for preparing an intravenous injection using a vial and MINI-BAG Plus container. It shows removing and disinfecting the vial cover, peeling foil from the bag, inspecting for moisture, attaching the drug vial adaptor, and pushing the adaptor down firmly onto the vial. The diagram highlights vial closure, drug vial, bag, administration port, and adaptor components.*

FDA Label Image

Reconstitution Pictures 4, 5 And 6 (Image 02)

An instructional diagram showing preparation steps for intravenous sodium chloride injection. It illustrates squeezing and checking vial seals, bending to break seals, holding and squeezing solution from a vial into a bag, suspending drug in solution, and forcing solution from the bag into a vial when preparing liquid drug vials.*

FDA Label Image

0.9% Sodium Chloride Injection Usp Container Label Ndc 0338-0553-11 (Image 03)

Label for 0.9% Sodium Chloride Injection USP in a 50 mL Mini-Bag Plus Container by Baxter Healthcare Corporation. The label includes dosage information, pH, osmolality, usage cautions, and manufacturer details. It instructs to break the seal and mix before use.*

FDA Label Image

0.9% Sodium Chloride Injection Usp Carton Label Ndc 0338-0553-11 (Image 04)

Label for 0.9% Sodium Chloride Injection, USP in a mini-bag plus container, quantity 80-50 mL. The label includes the NDC number 0338-0553-11, lot number, expiration date, a barcode, and the product name in uppercase letters.*

* 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.