Potassium Chloride Injection, Solution
Product Images NDC 0338-0703

6 FDA label images from Baxter Healthcare Corporation · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 0338-0703). 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

Potassium Chloride Injection Representative Container Label Ndc 0338-0703-41 (Image 01)

Potassium Chloride Injection Representative Container Label Ndc 0338-0703-41 (Image 01)
Potassium Chloride Injection label from Baxter Healthcare Corporation, showing a highly concentrated solution with strength 20 mEq per 50 mL. The label specifies each 50 mL contains 1.49 g Potassium Chloride in a sterile single dose container. It includes storage instructions and administration warnings for intravenous use with calibrated infusion devices, emphasizing use by central route when possible.*
FDA Label Image

Potassium Chloride Injection Representative Carton Label Ndc 0338-0703-41 (Image 02)

Potassium Chloride Injection Representative Carton Label Ndc 0338-0703-41 (Image 02)
Label for Potassium Chloride Injection showing a strength of 20 mEq per 50 mL vial. The label includes lot number, expiration date, NDC 0338-0703-41, and barcode information. It is a solution for intravenous administration by Baxter Healthcare Corporation.*
FDA Label Image

Potassium Chloride Injection Representative Container Label Ndc 0338-0705-41 (Image 03)

Potassium Chloride Injection Representative Container Label Ndc 0338-0705-41 (Image 03)
Potassium Chloride Injection label showing a highly concentrated solution at 200 mEq/L with a strength of 10 mEq per 50 mL. The label notes it is a sterile single dose container, hypertonic with 400 mOsmol/L, for intravenous use, and emphasizes use only with a calibrated infusion device via the central route. Manufactured by Baxter Healthcare Corporation in the USA.*
FDA Label Image

Potassium Chloride Injection Representative Carton Label Ndc 0338-0705-41 (Image 04)

Potassium Chloride Injection Representative Carton Label Ndc 0338-0705-41 (Image 04)
Label for Potassium Chloride Injection, 10 mEq per 50 mL intravenous solution. The label includes a lot number, expiration date, product code, and NDC 0338-0705-41. Barcodes are present below the product information. The label is from Baxter Healthcare Corporation.*
FDA Label Image

Potassium Chloride Injection Representative Container Label Ndc 0338-0707-48 (Image 05)

Potassium Chloride Injection Representative Container Label Ndc 0338-0707-48 (Image 05)
Potassium Chloride Injection label displaying a strength of 10 mEq per 100 mL in a sterile single-dose container. The label includes the product's high concentration warning (100 mEq/L), instructions for use, storage conditions at room temperature, and manufacturer information as Baxter Healthcare Corporation, USA. The NDC number 0338-0709-48 is also visible.*
FDA Label Image

Potassium Chloride Representative Carton Label 0338-0707-48 (Image 06)

Potassium Chloride Representative Carton Label  0338-0707-48 (Image 06)
Potassium Chloride Injection label showing 10 mEq per 100 mL strength. The label includes lot number, expiration date placeholder, and barcode. The product is indicated for intravenous use with an NDC of 0338-0709-48. The label displays the code 2B0826 and quantity information (24-100 mL).*

* 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.