Sodium Acetate Injection, Solution, Concentrate
Product Images NDC 0409-7299

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 Sodium Acetate (NDC 0409-7299). 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

Logo (Sodium Acetate 01)

FDA Label Image

Principal Display Panel (20 mL Vial Label)

Principal Display Panel (20 mL Vial Label)
Label for Sodium Acetate Injection USP, 40 mEq/20 mL (2 mEq/mL), single-dose vial. The label states it is for intravenous use, must be diluted, and includes storage instructions. Distributed by Hospira, Inc., the label also shows NDC 0409-7299-83 and additional formulation details such as pH and sterility.*
FDA Label Image

Principal Display Panel (20 mL Vial Tray)

Principal Display Panel (20 mL Vial Tray)
The packaging label for Sodium Acetate Injection, USP, 40 mEq/20 mL (2 mEq/mL) solution concentrate for intravenous use. The single-dose 20 mL vial label includes usage caution "MUST BE DILUTED," a barcode, Hospira, Inc. as the labeler, and storage instructions. The label highlights its use by intravenous route and emphasizes aseptic technique.*

* 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.