Lidopro Patch (lidocaine 4%, Menthol 1%) Patch
Product Images NDC 83881-402

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Lidopro Patch (lidocaine 4%, Menthol 1%) (NDC 83881-402). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Clinic Pharma, 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

402-15 (Rs 15 Lidopro Patch Carton 15 010625)

402-15 (Rs 15 Lidopro Patch Carton 15  010625)
The packaging label for LidoPro Patch features the proprietary name prominently on a teal background with a molecular pattern design. The label specifies this as a pain relieving patch, containing 15 patches measuring 10 cm by 12 cm. The product is labeled with the NDC 83881-402-15, manufactured by Clinic Pharma, with details of active ingredients lidocaine 4% and menthol 1%. Additional product and usage information is provided on the label's text panel.*
FDA Label Image

402-05 (Rs Lidopro Patch Pouch 010625)

402-05 (Rs Lidopro Patch Pouch   010625)
LidoPro patch Pain Relieving Patch with active ingredients Lidocaine 4% and Menthol 1%. The front packaging is teal with molecular pattern graphics and lists three benefits: Deep Penetrating, Long-lasting, Soothing. Each box contains 5 patches measuring 10 cm x 12 cm (3.9" x 4.7"). The back label includes detailed Drug Facts, warnings, directions, inactive ingredients, contact information, and is manufactured for Clinic Pharma, Las Vegas, NV 89121.*

* 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.