Dermacinrx Zrm Pak Kit
Product Images NDC 59088-805

3 FDA label images from Puretek Corporation · 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 Dermacinrx Zrm Pak (NDC 59088-805). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Puretek Corporation, 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

Image Description (Figure 1)

Image Description (Figure 1)
A line graph depicting plasma lidocaine concentration (ng/mL) over time (hours) up to 72 hours. The graph shows three peaks in plasma lidocaine levels occurring approximately every 24 hours, with concentrations ranging from near 0 to over 100 ng/mL. The x-axis is labeled 'Hours' and the y-axis is labeled 'Plasma Lidocaine, ng/mL.'*
FDA Label Image

Image Description (Lidocaine Structure)

Image Description (Lidocaine Structure)
Chemical structure of lidocaine, comprised of aromatic, amide, and amine functional groups, as shown in a line and letter diagram with substituents including methyl and ethyl groups.*
FDA Label Image

Image Description (Zrm Pak V5)

Image Description (Zrm Pak V5)
Packaging label for DermacinRx ZRM Pak, a prescription kit containing lidocaine 5% patches (15 count) and a Skin Repair Complex dimethicone cream 5% in a 4 fl oz (118 mL) container. The label features the brand name, dosage strengths, components, and PureTek Corporation as the labeler, with instructions to store at 20° to 25°C and to keep medication out of reach of children.*

* 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.