Derma Numb Pain Relief Gel
Product Images NDC 70188-005

2 FDA label images from A.t.s. Laboratories, Llc · 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 Derma Numb Pain Relief (NDC 70188-005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A.t.s. Laboratories, 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.

Product Images & Figures Index

FDA Label Image

1oz Label (1oz Label)

1oz Label (1oz Label)
Drug Facts panels for Derma Numb Pain Relief 40 mg/g Lidocaine HCL topical gel by A.T.S. Laboratories, LLC. The panels detail active ingredient information, uses for temporary pain and itching relief, warnings for external use and avoiding contact with eyes, directions for application 3-4 times daily for ages 2 and older, other protective information, inactive ingredients list, and a customer questions phone number. The label also includes a small product representation showing the brand name and packaging size of 1 oz.*
FDA Label Image

4oz Label (4oz Label)

4oz Label (4oz Label)
The packaging label for Derma Numb Pain Relief Spray Gel contains Lidocaine HCL 40 mg/g as the active ingredient. It is a topical gel manufactured by A.T.S. Laboratories, LLC. The label prominently features the product name in blue and black text on a white background with blue accents and indicates a 4 oz. container. The Drug Facts panel lists usage, warnings, directions, inactive ingredients, and contact information for questions or comments.*

* 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.