Lmd In Sodium Chloride Injection, Solution
Product Images NDC 0409-7419

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Lmd In Sodium Chloride (NDC 0409-7419). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, Inc., 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

Structural Formula Dextrose (Lmd 01)

Chemical structure of the active ingredient dextran 40, as depicted in the image. The diagram shows the molecular connectivity characteristic of dextran polymers, which is consistent with the ingredient in LMD in Sodium Chloride injection solution by Hospira, Inc.*

FDA Label Image

Hospira Logo (Lmd 02)

FDA Label Image

Bag Ndc 0409-7418-13 (Lmd 03)

Label for LMD in Sodium Chloride 10% Injection, solution in 500 mL packaging by Hospira, Inc. The product contains Dextran 40 in Dextrose Injection, USP, with each 100 mL containing 10g Dextran 40 and 5g Dextrose. Intended for intravenous use, the label includes usage, storage, and safety information and notes it is a single-dose container.*

FDA Label Image

Principal Display Panel (500 mL Bag Pouch Case Overwrap)

Container label for LMD in Sodium Chloride injection, solution, showing instructions to open at notch, handling directions including to keep the solution sterile and avoid excessive heat, a HDPE recycling symbol, and the statement that it is not made with natural rubber latex. No dosage or strength information is visible on this label.*

FDA Label Image

Bag Ndc 0409-7419-14 (Lmd 05)

Label for LMD in Sodium Chloride injection, 10% strength, containing 10 g Dextran 40 per 100 mL in 0.9% sodium chloride. The 500 mL intravenous solution is distributed by Hospira, Inc. The label includes cautions like no additive medications via plasma volume expanders and storage instructions. The label also notes no bacteriostat and single-dose container.*

FDA Label Image

Principal Display Panel (500 mL Bag Pouch Case Overwrap)

Packaging label for LMD in Sodium Chloride Injection, Solution, intravenous, 10 g/100 mL, by Hospira, Inc. The label includes usage instructions to tear at the notch and warnings about not removing the overwrap until ready for use. It advises checking for leaks and discarding if sterility is impaired. It also mentions storage at room temperature (25°C), avoiding excessive heat, and that it is not made with natural rubber latex. The HDPE recycling symbol is present.*

* 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.