Vasopressin In 0.9% Sodium Chloride Injection
Product Images NDC 0338-9647

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Vasopressin In 0.9% Sodium Chloride (NDC 0338-9647). 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

Vasopressin Structural Formula (Image 01)

Chemical structure diagram showing the amino acid sequence of vasopressin, including cysteine, tyrosine, phenylalanine, glutamine, aspartic acid, proline, arginine, and glycine residues.*

FDA Label Image

Representative Container Label Ndc 0338-9640-12 Panel 1 Of 2 (Image 02)

Label for Vasopressin in 0.9% Sodium Chloride Injection, 20 units per 100 mL (0.2 units/mL), intravenous infusion. This single-dose 100 mL container is sterile and labeled for refrigerated storage (2°C to 8°C). Manufactured by Baxter Healthcare Corporation, the label includes usage and storage instructions, emphasizing protection from light and freezing.*

FDA Label Image

Representative Container Label Ndc 0338-9640-12 Panel 2 Of 2 (Image 03)

This panel contains text instructing placement of a barcode, specifying 'BAR CODE POSITION ONLY UPC-A' and displaying a placeholder barcode made of Xs. The background is light pink, and the text is centered within a bordered box.*

FDA Label Image

Representative Container Label Ndc 0338-9647-12 Panel 1 Of 2 (Image 04)

Label for Vasopressin in 0.9% Sodium Chloride Injection, 40 units per 100 mL (0.4 units/mL), single-dose 100 mL intravenous infusion container. Label includes storage instructions (refrigerate 2-8°C, protect from light and freezing), usage directions, and manufacturer information (Baxter Healthcare Corporation).*

FDA Label Image

Representative Container Label Ndc 0338-9647-12 Panel 2 Of 2 (Image 05)

Label for Vasopressin in 0.9% Sodium Chloride injection, showing a placeholder for a barcode with text indicating 'BAR CODE POSITION ONLY UPC-A' and a series of X's representing the barcode base. No additional product information is visible on the label.*

FDA Label Image

Representative Carton Label Ndc 0338-9640-12 Panel 1 Of 2 (Image 06)

Vasopressin in 0.9% Sodium Chloride Injection 20 units per 100 mL label from Baxter Healthcare Corporation. The label instructs storage refrigerated at 2°C to 8°C (36°F to 46°F) and use within 72 hours once removed from refrigeration. It contains 6 single-dose 100 mL bags and includes barcode positioning information. The product is designated Rx only.*

FDA Label Image

Representative Carton Label Ndc 0338-9640-12 Panel 2 Of 2 (Image 07)

This image shows a text panel for Vasopressin in 0.9% Sodium Chloride injectable solution for intravenous infusion. It details the strength as 0.2 units/mL, additional ingredients including sodium chloride and sodium DL-lactate, and mentions pH adjustment. The panel notes Baxter Healthcare Corporation as the manufacturer.*

FDA Label Image

Representative Carton Label Ndc 0338-9647-12 Panel 1 Of 2 (Image 08)

Packaging label of Vasopressin in 0.9% Sodium Chloride Injection, showing 40 units per 100 mL (0.4 units/mL) strength. The label includes storage instructions to refrigerate at 2°C to 8°C (36°F to 46°F) and use within 72 hours once removed. It indicates the product contains six 100 mL single-dose bags and is labeled by Baxter Healthcare Corporation.*

FDA Label Image

Representative Carton Label Ndc 0338-9647-12 Panel 2 Of 2 (Image 09)

Label for Vasopressin in 0.9% Sodium Chloride injection, intravenous use, containing 0.4 units/mL strength. The label includes dosage information referencing prescribing details and mentions inactive ingredients such as sodium chloride and sodium DL-lactate. The product is labeled by Baxter Healthcare Corporation, Deerfield, IL, with NDC 0338-9647-12 and code 2G3499.*

* 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.