Diprivan Injection, Emulsion
Product Images NDC 65219-800

5 FDA label images from Fresenius Kabi Usa, Llc · 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 Diprivan (NDC 65219-800). 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.

FDA Label Image

Dipr Struct (Dip0f 0004 01)

Dipr Struct (Dip0f 0004 01)
Chemical structure of propofol, showing its molecular formula C12H18O and molecular weight 178.27. The diagram features a benzene ring with two isopropyl groups and one hydroxyl group attached.*
FDA Label Image

Dip Grf (Dip0f 0004 02)

Dip Grf (Dip0f 0004 02)
Line graph depicting plasma propofol concentration over time in minutes after the end of infusion for Diprivan 10 mg/mL intravenous injection. The graph shows curves for recovery after 1 hour, 10 hour, and 10 day infusion durations, with a dashed line indicating the awakening plasma concentration level.*
FDA Label Image

Logo (Dip0f 0004 03)

FDA Label Image

Vialrfid (Dip0f 0004 04)

Vialrfid (Dip0f 0004 04)
Diprivan (Propofol) Injectable Emulsion USP 200 mg per 20 mL (10 mg per mL) is an intravenous injection labeled for human prescription use. The label indicates a 20 mL single-dose vial, instructs to shake well before using, and includes a warning about EDTA inhibiting microbial growth for up to 12 hours after opening. Manufactured by Fresenius Kabi USA, LLC, made in Sweden, with storage instructions to keep between 4° to 25°C and not to freeze.*
FDA Label Image

Carton (Dip0f 0004 05)

Carton (Dip0f 0004 05)
Packaging label for Diprivan (Propofol) injectable emulsion USP, 200 mg per 20 mL (10 mg per mL) for intravenous administration. The box contains ten 20 mL single-dose vials. Labeler is Fresenius Kabi USA, LLC. The label includes instructions to shake well before using and warnings about aseptic technique and EDTA to inhibit microbial growth.*

* 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.