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

View Photos of 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 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

FDA Label Image

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

Potassium Chloride And Sodium Chloride Representative Container Label  Ndc 0338-0704-34 (Image 02)
This is a description of a medical product, which appears to be a 1000 mL container of 0.45% sodium chloride solution, with the addition of 20 milliequivalents of potassium chloride. The container is packaged in a VIAFLEX PLUS container, and contains a lot number and an expiration date. There are also two barcodes present on the container, one of which is a secondary barcode labeled with the characters "KXXXX," and another primary barcode labeled with the characters "(01) 50303380704342".*
FDA Label Image

Image 03

Image 03
This is a description of a potassium chloride solution used for healthcare purposes. The solution contains potassium chloride and 0.9% sodium chloride. The container is a single dose and should be used with aseptic technique. The inner bag should be inspected and discarded if any leaks are found. This product is distributed in Canada by Baxter Corporation and trademarks include Baxter Viaflex and PL 146. For product information, customers can call 1-800-933-0303.*
FDA Label Image

Image 04

Image 04
This is a description of a medical product, specifically a VIAFLEX® PLUS CONTAINER that contains 20 MEQ POTASSIUM CHLORIDE IN 0.9% SODIUM CHLORIDE INJ. The product has a secondary bar code and a lot primary bar code with specific identifiers for tracking and tracing purposes. The product also has a unique identification number (01) 50303380691048.*
FDA Label Image

Image 05

Image 05
This appears to be a product label for a 1000 mL bag of 0.9% Sodium Chloride Injection USP solution containing Sodium Chloride, Potassium Chloride, and Chloride. The bag is designed for single dose use only. Additives may be incompatible and consulting a pharmacist is recommended. The bag should be stored in a moisture barrier overwrap at room temperature until ready to use and excessive heat should be avoided. The product should be administered as directed by a physician and caution should be taken to inspect the inner bag for leaks before use. The text also includes company and trademark information, a phone number for product information, and distribution information for Canada and the USA.*
FDA Label Image

Image 06

Image 06
This is a description of a medical product in a 1000 ML VIAFLEX PLUS CONTAINER. It contains 40mEq POTASSIUM CHLORIDE mixed with 0.9% SODIUM CHLORIDE injection, with secondary and primary barcodes for identification. There is an expiration date marked as "EXP" but the actual date is not provided due to XXXXX being used in place of actual figures, suggesting that the text may have been redacted.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.