Bupivilog Kit
Product Images NDC 80425-0353

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bupivilog Kit (NDC 80425-0353). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Of Tennessee, 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

Label 1 (Bupivilog Kit 80425 0353 01)

Label 1 (Bupivilog Kit 80425 0353 01)
Label for Bupivilog Kit, a prescription drug kit containing marcaine, kenalog, and povidone iodine. The label includes the NDC 80425-0353-01, lot number, and expiration date 7/28/2023. The product is labeled for multiple administration routes including epidural, intra-articular, intramuscular, and topical. Manufactured by Advanced Rx of Tennessee, LLC in Nashville, Tennessee.*
FDA Label Image

Image Description (Bupivacaine Str)

Image Description (Bupivacaine Str)
Chemical structure of the active ingredients in Bupivilog Kit, showing molecular components including hydrochloride (HCl) and hydrate (H2O) groups. The structure depicts part of the molecule with amide and aromatic ring features typical of the drug components marcaine, kenalog, and povidone iodine.*
FDA Label Image

Structure (Triamcinolone Acetonide Str)

Structure (Triamcinolone Acetonide Str)
Chemical structure diagram showing a complex steroid molecule with multiple hydroxyl, ketone, and fluoro substituents. This structure corresponds to the active ingredient, likely one of the generic components such as a corticosteroid present in Bupivilog Kit.*

* 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.