Lm Plus Relief Patch
Product Images NDC 71436-3571

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 Lm Plus Relief (NDC 71436-3571). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ari Brands, 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

Lidocaine (Lm Plus Relief Patch 01)

Lidocaine (Lm Plus Relief Patch 01)
Chemical structure diagram of the active ingredient lidocaine, showing standard molecular bonds and atom connectivity consistent with lidocaine's known chemical composition.*
FDA Label Image

Menthol (Lm Plus Relief Patch 02)

Menthol (Lm Plus Relief Patch 02)
Chemical structure of the active ingredient in LM Plus Relief, lidocaine and menthol. The image shows a molecular diagram featuring a cyclohexane ring with hydroxyl and methyl groups attached, characteristic of menthol molecule.*
FDA Label Image

Ndc 71436-3571-5lm Plus Relief Patchdispense By Prescriptionlidocaine 3.5% + Menthol 7%15 Patches (Lm Plus Relief Patch 03)

Ndc 71436-3571-5lm Plus Relief Patchdispense By Prescriptionlidocaine 3.5% + Menthol 7%15 Patches (Lm Plus Relief Patch 03)
The packaging label for LM Plus Relief Patch, containing 490 mg and 980 mg strengths of Lidocaine and Menthol in a topical patch dosage form. The label includes Drug Facts with active ingredients, uses, warnings, directions, and inactive ingredients. The labeler is ARI BRANDS, LLC. The design features a graphic of a knee joint on the front panel and the NDC 71436-3571-5 along with barcodes and manufacturing information.*

* 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.