Synoflex Patch
Product Images NDC 70512-015

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Synoflex Patch (NDC 70512-015). 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

Snyoflex (Synoflex Carton 2)

Snyoflex (Synoflex Carton 2)
This is a prescription lidocaine HCl 4% and menthol 5% patch used for temporary relief of pain. It is for external use only, and should not be used on puncture wounds, cut, irritated, or swollen skin. The patch should not be applied to wounds or damaged, broken, or irritated skin, and contact with eyes or mucous membranes should be avoided. Tightly bandaging or applying local heat should be avoided. If the condition worsens or redness is present, or irritation develops, one should stop using the patch and ask a doctor. The patch should be disposed of away from children and pets. Pregnant individuals should consult with a healthcare professional before use. The affected area should be cleaned and dried, and one patch should be used for up to 12 hours. Children 12 years or younger should consult with a doctor. The product should be protected from excessive moisture and direct sunlight. The adhesive used is acrylic adhesive. This product is manufactured by Sola Pharmaceuticals LLC in Baton Rouge, Louisiana.*

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