Lipiodol Injection
Product Images NDC 67684-1901

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lipiodol (NDC 67684-1901). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Guerbet 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

Carton 4 8

Packaging label for Lipiodol Ultra-Fluide (Ethiodized Oil) Injection, 4.8 g iodine per 10 mL (480 mg iodine per mL), sterile liquid, in a 10 mL vial. The label includes administration instructions, storage conditions, lot and expiration dates, and the labeler Guerbet LLC. The product is for intrauterine, intralymphatic, selective hepatic intra-arterial administration only and is for single use.*

FDA Label Image

Image Of The Ampuole Label (Lipiodol Amp)

Label for Lipiodol Ultra-Fluide (Ethiodized Oil) Injection, 480 mg iodine per mL (4.8 g per 10 mL), intended for intrauterine, intralymphatic, and selective hepatic intra-arterial administration. The 10 mL vial label includes manufacturer Guerbet LLC and usage instructions noting single use and light protection.*

FDA Label Image

Image Of The Carton (Lipiodol Carton)

Packaging label for Lipiodol Ultra-Fluide (Ethiodized Oil) Injection, containing 480 mg iodine per mL (4.8 g iodine per 10 mL) in a 10 mL ampoule. The label indicates it is a sterile liquid for injection and includes usage restrictions for intrauterine, intralymphatic, and selective hepatic intra-arterial administration only. Manufactured for Guerbet LLC and distributed by Guerbet LLC, Princeton, New Jersey. The label also provides storage instructions and cautions for single use only, discarding unused portions.*

FDA Label Image

Vial 4 8

Label for Lipiodol Ultra-Fluide 480 mg/mL (4.8 g iodine per 10 mL) injection by Guerbet LLC. The label specifies administration routes as intrauterine, intralymphatic, and selective hepatic intra-arterial. It includes usage instructions to protect from light and for single use only. The package size is 10 mL.*

* 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.