Propofol Injection, Emulsion
Product Images NDC 0641-6195

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Propofol (NDC 0641-6195). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Structure (Propofol Injectable Emulsion Usp 1)

Chemical structure of propofol showing a benzene ring with two isopropyl groups and a hydroxyl group attached.*

FDA Label Image

Graph (Propofol Injectable Emulsion Usp 2)

A line graph depicting plasma propofol concentration (mg/mL) over time (minutes) after the end of infusion, showing recovery after 10-day, 1-hour, and 10-hour infusions. The graph illustrates concentration decline and a target plasma concentration line along with awakening time.*

FDA Label Image

462-843-00 (Propofol Injectable Emulsion Usp 3)

Label for Propofol Injectable Emulsion USP, 200 mg per 20 mL (10 mg per mL) intravenous injection emulsion by Hikma Pharmaceuticals USA Inc. The label notes it contains benzyl alcohol, is for single patient use only, and includes storage instructions along with a warning to shake well before using.*

FDA Label Image

462-844-00 (Propofol Injectable Emulsion Usp 4)

Label for Propofol Injectable Emulsion, USP 200 mg per 20 mL (10 mg per mL) intravenous injection emulsion by Hikma Pharmaceuticals USA Inc. The label states it contains benzyl alcohol, is for single patient use, and must be shaken well before using. Detailed drug content and storage instructions are included, with warnings about aseptic technique and microbial growth inhibition.*

FDA Label Image

462-845-00 (Propofol Injectable Emulsion Usp 5)

Label for Propofol Injectable Emulsion, USP, 500 mg per 50 mL (10 mg per mL) intravenous injection. The label specifies single-patient use and contains benzyl alcohol. Manufactured by Hikma Pharmaceuticals USA Inc., Eatontown, NJ. The label includes dosage and storage information, warnings for aseptic technique, and handling instructions.*

FDA Label Image

462-846-00 (Propofol Injectable Emulsion Usp 6)

Label for Propofol Injectable Emulsion, USP 500 mg per 50 mL (10 mg per mL) for intravenous administration. The product contains benzyl alcohol and is intended for single patient use. The label includes storage instructions, warnings about aseptic technique, and manufacturer information for Hikma Pharmaceuticals USA Inc. The packaging specifies 20 vials of 50 mL each.*

FDA Label Image

462-847-00 (Propofol Injectable Emulsion Usp 7)

Label for Propofol Injectable Emulsion USP 1 gram per 100 mL (10 mg/mL), an intravenous injection by Hikma Pharmaceuticals USA Inc. The label highlights that it contains benzyl alcohol and is for single patient use only. It includes storage instructions, a dosage note to see the package insert, and warnings about aseptic technique and benzyl alcohol content.*

FDA Label Image

462-848-00 (Propofol Injectable Emulsion Usp 8)

Label of Propofol Injectable Emulsion, USP 1 gram per 100 mL (10 mg per mL) by Hikma Pharmaceuticals USA Inc. This intravenous injection emulsion is supplied in 10 x 100 mL vials. The label includes cautionary information about use, storage between 4° to 25°C, and that it contains benzyl alcohol and no preservatives. It instructs to shake well before use and emphasizes single patient use.*

FDA Label Image

Serialization Image Layout 1 (Propofol Injectable Emulsion Usp 9)

A product label for PROPOFOL injection, emulsion, 10 mg/mL by Hikma Pharmaceuticals USA Inc. The label includes a QR code and displays serialization data including GTIN, serial number, expiration date, and lot number in a standardized format.*

* 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.