Sodium Acetate Injection, Solution, Concentrate
Product Images NDC 63323-032

4 FDA label images from Fresenius Kabi Usa, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sodium Acetate (NDC 63323-032). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Figure (Sod0i 0002 01)

Figure (Sod0i 0002 01)
An instructional diagram demonstrating how to use a sling with material. It depicts step-by-step illustrations showing hand placement, folding and securing the sling around the arm and hand for support.*
FDA Label Image

Figure (Sod0i 0002 02)

Figure (Sod0i 0002 02)
FDA Label Image

Package Label (PRINCIPAL DISPLAY – Sodium Acetate 400 mEq per 100 mL Vial Label)

Package Label (PRINCIPAL DISPLAY – Sodium Acetate 400 mEq per 100 mL Vial Label)
Sodium Acetate Injection, USP label indicating a concentration of 400 mEq per 100 mL (4 mEq per mL). The label includes warnings such as 'Pharmacy Bulk Package - Not for Direct Infusion' and 'Caution: Must Be Diluted.' It specifies intravenous use only, container volume of 100 mL, and is Rx only.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – Sodium Acetate 400 mEq per 100 mL Tray Label)

Package Label (PRINCIPAL DISPLAY – Sodium Acetate 400 mEq per 100 mL Tray Label)
Sodium Acetate Injection, USP 400 mEq per 100 mL (4 mEq per mL) intravenous solution. The label indicates the product is a pharmacy bulk package not for direct infusion, containing 20 vials of 100 mL each. The labeler is Fresenius Kabi USA, LLC.*

* 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.