Siyntherma Plus
Product Images NDC 72835-102

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Siyntherma Plus (NDC 72835-102). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by V2 Pharma, 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

Myderm Freeze (Myderm Pro Freeze Cooling Menthol Is0252)

Packaging label for Siyntherma Plus by V2 Pharma, LLC. The label highlights the product as a 3 FL OZ (89 mL) cooling menthol pain relief roll-on with 50% more menthol. The label features 'myDerm PRO FREEZE' branding and includes a detailed drug facts panel listing menthol 6% as the active ingredient with topical analgesic purpose, along with warnings, directions, and inactive ingredients.*

FDA Label Image

Syntherma Plus (Syntherma Plus Packaging)

The packaging label for Syntherma Plus by V2 Pharma, LLC features a green and blue wave design. The label indicates the product includes Lidocaine Patch 5% (30 count) and Menthol USP 6% Roll-On Gel (3 oz). It states the product is Rx Only with NDC 72835-102-02 and provides storage instructions and manufacturer information.*

FDA Label Image

Chemical Structure (Lidocaine Patch 1)

Chemical structure diagram of a compound showing a substituted benzene ring with two methyl groups, linked via an amide bond to an ethylene chain attached to a nitrogen atom bonded to two ethyl groups. This likely represents the active ingredient associated with Siyntherma Plus by V2 Pharma, LLC.*

FDA Label Image

Figure 1 (Lidocaine Patch 2)

A line graph showing plasma lidocaine concentration (ng/mL) over time (hours) with peaks and troughs repeating approximately every 24 hours, indicating cyclic plasma levels. The y-axis measures plasma lidocaine in ng/mL, and the x-axis measures time in hours from 0 to 72.*

FDA Label Image

Pouch Front (Lidocaine Patch 3)

The image shows a label for a Lidocaine Patch 5% containing 700 mg lidocaine per patch (50 mg per gram adhesive) in an aqueous base with methylparaben and propylparaben as preservatives. The label instructs storage conditions and warns to keep patches out of reach of children and pets. Manufactured and distributed by Amneal Pharmaceuticals, the label also notes the patch size as 10 cm x 14 cm and indicates it is prescription only.*

FDA Label Image

Gh (Lidocaine Patch 4)

The image shows the 'Directions for Use' for Siyntherma Plus, a lidocaine patch. Instructions include cutting the patch envelope along the dotted line, removing the transparent release liner before application, and applying patches only once for up to 12 hours within a 24-hour period. Additional instructions advise against placing external heat sources over the patch and avoiding water contact to prevent detachment. Users are also instructed to fold used patches with the adhesive side sticking to itself before discarding.*

FDA Label Image

Carton (Lidocaine Patch 5)

Packaging label of Lidocaine Patch 5% showing product name, active ingredient strength, and package quantity of 30 patches. Label includes storage instructions, warnings, and dosage directions. The labeler shown is Amneal Pharmaceuticals with locations in Piscataway, NJ, and Glasgow, KY. The packaging also has pictorial instructions for use and barcode details.*

* 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.