Hetastarch In Sodium Chloride Injection, Solution
Product Images NDC 0409-7248

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hetastarch In Sodium Chloride (NDC 0409-7248). 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 Hetastarch (Hetastarch 01)

Chemical structure diagram showing a cyclic molecule with various hydroxyl (OH) groups and substituents labeled as R2, R3, R6, and repeating unit notation (n), representing the chemical structure of Hetastarch, the active ingredient in Hetastarch in Sodium Chloride injection solution.*

FDA Label Image

Hospira Logo (Hetastarch 02)

FDA Label Image

Bag Ndc 0409-7248-13 (Hetastarch 03)

Label for Hetastarch in Sodium Chloride 6% injection, solution in a 500 mL plastic IV bag. The label shows the active ingredient Hetastarch 6 g per 100 mL in 0.9% sodium chloride, for intravenous use only. The product is distributed by Hospira, Inc., Lake Forest, Illinois. The bag includes dosage details and usage instructions with visible volume markings and connector ports at the bottom.*

FDA Label Image

Hetastarch 04

A drug label panel providing instructions to open at the notch and cautions not to remove the overwrap until ready for use. It advises checking for leaks by squeezing the container and discarding if leaks are found, as sterility may be impaired. Storage recommendations include room temperature (25°C), avoiding excessive heat, and protecting from freezing. The label also states the product is not made with natural rubber latex and includes an HDPE recycling symbol.*

* 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.