Propofol Lipuro
Product Images NDC 0264-4850

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Propofol Lipuro (NDC 0264-4850). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by B. Braun Medical 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

Diprivan Labels (Propofol Lipuro 1)

Diprivan Labels (Propofol Lipuro 1)
Labels for DIPRIVAN (Propofol) injectable emulsion, USP in strengths of 1000 mg per 100 mL, 500 mg per 50 mL, and 200 mg per 20 mL. Each label indicates the product is for intravenous administration, single patient use only, and includes directions to shake well before using. Manufactured by Fresenius Kabi USA, LLC in Austria, the labels also mention the inclusion of EDTA as a preservative and caution on microbial growth inhibition and discard timing after opening.*
FDA Label Image

Propofol Label (Propofol Lipuro 2)

Propofol Label (Propofol Lipuro 2)
Label for Propofol-Lipuro 10 mg/ml emulsion for injection or infusion by B. Braun Medical Inc. The label states the concentration as 1000 mg in 100 ml (1%) and includes usage instructions indicating intravenous administration. Ingredients include propofol, refined soya-bean oil, medium-chain triglycerides, glycerol, egg lecithin, sodium oleate, and water for injections. Warnings about storage and single patient use are present. Manufacturer details indicate B. Braun Melsungen AG, Germany.*
FDA Label Image

Vial Label (Propofol Lipuro 3)

Vial Label (Propofol Lipuro 3)
Propofol Lipuro 10 mg/ml injectable emulsion vial with a blue cap. The label shows the product name, concentration of 10 mg/ml, and packaging size of 1000 mg in 100 ml (1%). It is manufactured by B. Braun Medical Inc., with additional details including usage instructions and storage conditions visible on the label.*
FDA Label Image

Product Information (Propofol Lipuro 4)

Product Information (Propofol Lipuro 4)
A data table titled 'Product Information' specifying details about Propofol Lipuro. It lists the NDC number as 0264-4850-01, active ingredient as Propofol, strength as 1,000 mg in 100 mL (10 mg/mL concentration), and a single-dose vial fill volume of 100 mL. The table notes no antimicrobial retardant, excipients as a combination of medium- and long-chain triglycerides, vial size of 100 mL, 32 mm closure size, packaging as a pack of 10 single-dose vials, 24-month shelf life, storage instructions below 25°C without freezing, and manufacturer B. Braun Melsungen AG, Germany.*
FDA Label Image

Vial Label (Propofol Lipuro 5)

Vial Label (Propofol Lipuro 5)
Label for Propofol Lipuro 10 mg/ml emulsion for injection or infusion by B. Braun Medical Inc. The label states strength as 1000 mg in 100 ml (1%) with each ml containing 10 mg propofol. Ingredients include refined soya-bean oil, medium-chain triglycerides, glycerol, egg lecithin, and sodium oleate. The label includes administration instructions for intravenous use, storage guidelines, and manufacturer information from B. Braun Melsungen AG, Germany.*
FDA Label Image

Carton Label (Propofol Lipuro 6)

Carton Label (Propofol Lipuro 6)
Propofol-Lipuro 10 mg/ml (1%) emulsion for injection or infusion, with 1000 mg propofol in 100 ml vial. Pack of 10 vials, each containing 100 ml. Ingredients include propofol, refined soya-bean oil, medium-chain triglycerides, glycerol, egg lecithin, sodium oleate, and water for injections. Manufactured by B. Braun Melsungen AG, Germany. Label includes usage instructions and storage conditions.*

* 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.