Potassium Chloride In Sodium Chloride Injection, Solution
Product Images NDC 0338-0691

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Potassium Chloride In Sodium Chloride (NDC 0338-0691). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Company, 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

Image 01

Label for Potassium Chloride injection solution, 20 mEq strength in 1000 mL volume. The label states Potassium Chloride in 0.45% Sodium Chloride Injection USP. The product is offered by Baxter Healthcare Corporation, with detailed dosage and storage information on the label.*

FDA Label Image

Potassium Chloride And Sodium Chloride Representative Container Label Ndc 0338-0704-34 (Image 02)

Label for Potassium Chloride in Sodium Chloride injection, solution in a 1000 mL VIAFLEX PLUS container. It specifies 20 mEq Potassium Chloride in 0.45% Sodium Chloride Injection. The label includes placeholder fields for expiration date, lot number, and corresponding bar codes. The labeler is Baxter Healthcare Company.*

FDA Label Image

Image 03

Label for Potassium Chloride in 0.9% Sodium Chloride Injection USP, containing 20 mEq of Potassium Chloride per liter (20 mEq/L). The 1000 mL solution includes 900 mg sodium chloride and 150 mg potassium chloride per 100 mL. The label shows product details including lot, expiration, NDC 0338-0691-04, and manufacturer Baxter Healthcare Company in Deerfield, IL, USA, distributed in Canada by Baxter Corporation, Toronto, Ontario. Instructions and warnings are visible regarding sterile single-dose container use and storage conditions.*

FDA Label Image

Image 04

Label for Potassium Chloride in Sodium Chloride injection, solution in a VIAFLEX Plus container. The label states 20 mEq Potassium Chloride in 0.9% Sodium Chloride injection with a volume of 1000 mL. It includes expiration date, lot number, and primary and secondary barcode placeholders. No manufacturer name is visible on the label.*

FDA Label Image

Image 05

Label for Potassium Chloride Injection in 0.9% Sodium Chloride Injection USP, 40 mEq strength, in a 1000 mL single-dose container. The label includes detailed content of 900 mg sodium chloride and 300 mg potassium chloride per 100 mL, pH information, osmolarity, and storage instructions. Manufactured by Baxter Healthcare Company, USA, and distributed by Baxter Corporation, Canada.*

FDA Label Image

Image 06

Label for Potassium Chloride in Sodium Chloride injection, 40 mEq strength in a 1000 mL Viaflex Plus container. The label shows an expiration date and lot number area, along with primary and secondary barcode boxes. The solution contains 0.9% sodium chloride and potassium chloride, manufactured by Baxter Healthcare Company.*

* 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.