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Sodium Chloride
Product Images NDC 0409-6657
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 0409-6657). 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.
Principal Display Panel (20 mL Vial Label)
Label for Sodium Chloride 14.6% Injection, USP concentrate in a 20 mL single-dose vial. The label highlights it must be diluted for intravenous use and provides concentration details as 50 mEq/20 mL (2.5 mEq/mL). It is distributed by Hospira, Inc., Lake Forest, IL, USA.*
Principal Display Panel (20 mL Vial Tray)
Box packaging label for 14.6% Sodium Chloride Injection, USP, 50 mEq/20 mL (2.5 mEq/mL), single-dose vial. The label includes a red banner stating CONCENTRATE and a caution that it must be diluted for intravenous use. It indicates a 20 mL vial size with 25 units per carton. The labeler shown is Hospira, Inc.*
Principal Display Panel (40 mL Vial Label)
Label for Sodium Chloride Injection, USP concentrate 14.6% (100 mEq/40 mL) single-dose vial by Hospira, Inc. The label includes dosing information, caution for intravenous use after dilution, and distributor details in Lake Forest, IL, USA.*
Principal Display Panel (40 mL Vial Tray)
Sodium Chloride 14.6% Injection USP concentrate, 5.84 g/40 mL single-dose vial label by Hospira, Inc. The label highlights the product as a concentrate for intravenous use, including cautions for dilution, and states the strength as 100 mEq/40 mL (2.5 mEq/mL). The packaging includes manufacturer details and storage instructions.*
* 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.
