Lidaflex Patch
Product Images NDC 70512-012

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Lidaflex (NDC 70512-012). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sola Pharmaceuticals, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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FDA Label Image

Lidaflex (Lidaflex Patch Copy)

Lidaflex (Lidaflex Patch Copy)
This is a drug facts label for a topical pain patch containing Lidocaine HCI 4% as the active ingredient. This product is used for temporary pain relief and comes in a pack of 30 Flex patches that should be used no more than 3-4 times daily. The patch should not be used on wounds or damaged skin, and it is not recommended to use a heating pad with the patch. The user should not bandage the patch tightly and must avoid contact with the eyes, mucous membranes or rashes. If an allergic reaction occurs or the symptoms persist after 7 days, the user should stop using the patch and seek medical advice. The product should be kept out of reach of children and stored away from direct sunlight and excessive moisture. The product is manufactured by Sola Pharmaceuticals located in Baton Rouge, LA, and any queries can be directed to 866-747-7365.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.