Mannitol Injection, Solution
Product Images NDC 0990-7715

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mannitol (NDC 0990-7715). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Icu Medical 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

Chemical Structure (Mannitol 01)

Chemical Structure (Mannitol 01)
Chemical structure diagram of Mannitol showing its carbon backbone and attached hydroxyl groups consistent with the active ingredient in the product Mannitol injection solution.*
FDA Label Image

Principal Display Panel (250 mL Bag Label)

Principal Display Panel (250 mL Bag Label)
Label for Mannitol Injection, USP 20% solution in a 250 mL container, containing 50 g per 250 mL (200 mg/mL). The label includes usage instructions, warnings, and handling information. It is manufactured by ICU Medical Inc., with product NDC 0990-7715-12. The label shows volume calibration marks and various regulatory icons.*
FDA Label Image

Principal Display Panel (500 mL Bag Label)

Principal Display Panel (500 mL Bag Label)
Label for Mannitol 20% Injection, USP 100 g/500 mL (200 mg/mL), an intravenous injection solution. The 500 mL container label includes product information such as mannitol content per 100 mL, pH range, sterility status, and usage warnings. It also displays the labeler ICU Medical Inc. and symbols for latex content, recycling, and DEHP presence. The NDC 0990-7715-13 is printed near the top.*

* 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.