Mlk Kit F2 Kit
Product Images NDC 76420-742

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Mlk Kit F2 (NDC 76420-742). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Asclemed Usa, 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

Mlk00 0005 01

Chemical structure of an active ingredient shown with a piperidine ring connected to an amide group and a methyl-substituted aromatic ring, combined with hydrochloride and water molecules. Likely representing one of the components in MLK Kit F2.*

FDA Label Image

Mlk00 0005 02

Chemical structure of lidocaine, one of the active ingredients in the MLK Kit F2. The diagram shows the molecular formula with the aromatic ring, amide group, and ethyl substituents along with the hydrochloride (HCl) component.*

FDA Label Image

Mlk00 0005 03

Chemical structure of the active pharmaceutical ingredient shown in the MLK Kit F2 product. The diagram depicts the molecular structure with carbon rings, hydroxyl groups, fluorine atom, and multiple oxygen-containing functional groups.*

FDA Label Image

Mlk00 0005 04

This is a pharmaceutical kit with the NDC code 76420-742-01, available only with a prescription. The kit contains Bupivacaine HCl 0.5%, Lidocaine HCl Injection, USP 2%, Triamcinolone Acetonide Injectable Suspension, USP 40 mg/mL, Povidone-lodine Swabsticks, a pair of Nitrile Powder-Free Sterile Gloves, a drape, Adhesive Bandage, and Non-Sterile 4x4 Gauze. Needles and syringes are not included. It is a single-use kit designed for medical purposes. This kit has been manufactured in Torrance, CA 90501.*

* 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.