Propofol Injection, Emulsion
Product Images NDC 71288-729

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Propofol (NDC 71288-729). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal Pharmaceuticals 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

Principal Display Panel – Propofol Injectable Emulsion, Usp 1,000 mg Per 100 mL Carton (Prop 1000mg Carton V3)

Packaging label for Propofol Injectable Emulsion, USP, 1,000 mg per 100 mL (10 mg per mL) injection. The label indicates intravenous administration and contains 10 single-dose vials of 100 mL each. It is labeled by Meitheal Pharmaceuticals Inc. and includes instructions to shake well before use and discard within 12 hours of opening due to EDTA content.*

FDA Label Image

Principal Display Panel – Propofol Injectable Emulsion, Usp 1,000 mg Per 100 mL Container Label (Prop 1000mg Vial V3)

Label for Propofol Injectable Emulsion, USP 10 mg/mL (1,000 mg per 100 mL) single-dose vial by Meitheal Pharmaceuticals Inc. The label includes dosing information, usage instructions to shake well before use, and warnings against use if the vial is punctured or opened for over 12 hours. The product is for intravenous administration only.*

FDA Label Image

Principal Display Panel – Propofol Injectable Emulsion, Usp 200 mg Per 20 mL Carton (Prop 200mg Carton V3)

Propofol Injectable Emulsion USP 200 mg per 20 mL (10 mg per mL) carton label for intravenous administration by Meitheal Pharmaceuticals Inc. The label states the product is a single-dose vial (10 x 20 mL). It includes warnings to shake well before using and to use strict aseptic technique. The label also highlights the presence of EDTA, which inhibits microbial growth up to 12 hours after opening.*

FDA Label Image

Principal Display Panel – Propofol Injectable Emulsion, Usp 200 mg Per 20 mL Container Label (Prop 200mg Vial V3)

Propofol Injectable Emulsion, USP 10 mg/mL (200 mg per 20 mL) injection vial label by Meitheal Pharmaceuticals Inc. The 20 mL single-dose vial is for intravenous administration and labeled with storage instructions, microbial growth caution, and handling warnings. The label includes NDC 71288-729-20, lot and expiration date fields, and states the product is sterile and nonpyrogenic.*

FDA Label Image

Principal Display Panel – Propofol Injectable Emulsion, Usp 500 mg Per 50 mL Carton (Prop 500mg Carton V3)

Packaging label for Propofol Injectable Emulsion, USP, 500 mg per 50 mL (10 mg per mL) intravenous injection by Meitheal Pharmaceuticals Inc. The label includes dosing instructions, handling precautions, and storage information for 10 x 50 mL single-dose vials.*

FDA Label Image

Principal Display Panel – Propofol Injectable Emulsion, Usp 500 mg Per 50 mL Container Label (Prop 500mg Vial V3)

Label for Propofol Injection Emulsion, USP 500 mg per 50 mL (10 mg per mL) in a single-dose vial. The label includes a blue and white color scheme with red warning text to shake well before using. It indicates the drug is for intravenous use and prescription only. The labeler is Meitheal Pharmaceuticals Inc.*

FDA Label Image

Propofol Figure (Prop Figure)

A line graph showing plasma propofol concentration (mcg/mL) over time in minutes after the end of infusion. The graph compares recovery profiles for 1-hour, 10-hour, and 10-day infusions, indicating a target plasma concentration and the point of awakening.*

FDA Label Image

Structural Formula (Prop Structure)

Chemical structure of propofol, showing a phenol ring with two isopropyl groups (CH(CH3)2) attached and a hydroxyl (OH) group on the aromatic ring.*

* 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.