Propofol Injection, Emulsion
Product Images NDC 0069-0234

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Propofol (NDC 0069-0234). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pfizer Laboratories Div Pfizer 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

Chemical Structure (Propofol 01)

Chemical structure of Propofol, showing the hydroxyl group (OH) attached to a benzene ring and two isopropyl groups ((CH3)2CH and CH(CH3)2) as substituents on the aromatic ring.*

FDA Label Image

Figure (Propofol 02)

A line graph depicting plasma propofol concentration over time following different infusion durations (1 hour, 10 hours, and 10 days). The y-axis represents plasma propofol concentration in mcg/mL, and the x-axis shows minutes after the end of infusion. The graph includes a target plasma concentration level and indicates the awakening time relative to concentration decay.*

FDA Label Image

Logo (Propofol 03)

Label panel from Pfizer Propofol injection, emulsion, 10 mg/mL. The panel shows Pfizer logo and distributor information: Pfizer Laboratories Division of Pfizer Inc, New York, NY 10017. No other product details are visible on this label portion.*

FDA Label Image

Principal Display Panel (20 mL Vial Label)

Propofol Injectable Emulsion, USP 200 mg/20 mL (10 mg/mL) vial label for intravenous administration. The label includes storage instructions, usage warnings, and a barcode. Distributed by Pfizer Laboratories, the vial is sterile and nonpyrogenic with batch and expiry date fields.*

FDA Label Image

Principal Display Panel (20 mL Vial Carton)

Packaging label for Propofol Injectable Emulsion, USP 200 mg/20 mL (10 mg/mL) injection for intravenous administration by Pfizer Laboratories Div Pfizer Inc. The carton states 'Ten 20 mL Vials for Single Patient Use' and includes storage instructions, usage warnings, and a barcode. It also highlights use of strict aseptic technique and EDTA content limiting microbial growth to 12 hours after opening.*

FDA Label Image

Principal Display Panel (50 mL Vial Label)

Label for Propofol Injectable Emulsion USP, 10 mg/mL (500 mg/50 mL), an intravenous injection emulsion by Pfizer Laboratories. The label indicates storage instructions, dosage caution, and use of aseptic technique, highlighting that it contains EDTA which inhibits microbial growth for up to 12 hours after opening.*

FDA Label Image

Principal Display Panel (50 mL Vial Carton)

Packaging label for Propofol Injectable Emulsion, USP, 500 mg/50 mL (10 mg/mL) for intravenous use. The label shows that it contains twenty 50 mL vials for single patient use. Directions to shake well before using and warnings about aseptic technique and EDTA microbial inhibition are included. The labeler is Pfizer Laboratories Div Pfizer Inc.*

FDA Label Image

Principal Display Panel (100 mL Vial Label)

Label for Propofol Injectable Emulsion USP 1000 mg/100 mL (10 mg/mL) in a 100 mL single patient use vial for intravenous administration. The label includes storage instructions (4 to 25°C, do not freeze), a caution to use aseptic technique, and a note that the product contains EDTA which inhibits microbial growth up to 12 hours after opening. Distributed by Pfizer Laboratories Division of Pfizer Inc.*

FDA Label Image

Principal Display Panel (100 mL Vial Carton)

This is a packaging label for Propofol Injectable Emulsion, USP 1000 mg/100 mL (10 mg/mL) for intravenous administration. The label indicates it contains ten 100 mL vials for single patient use and is manufactured by Pfizer Laboratories Div Pfizer Inc. Important instructions include shaking well before use and using strict aseptic technique. The label also notes the emulsion contains EDTA to inhibit microbial growth and should be discarded within 12 hours of opening.*

* 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.