Derma Numb Pain Relief Gel
Product Images NDC 70188-005

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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.

FDA Label Image

1oz Label (1oz Label)

1oz Label (1oz Label)
This is a drug fact sheet for a Pain Relieving product named "DERMA". The active ingredients in this product are Lidocaine HOL__4.0% and wiw_External Avaosic L. These ingredients are helpful in providing temporary relief in cases of minor cuts, skin irritations or itching. Adults and children two-years or older are advised to apply the product to the affected area no more than 10 times a day. Children under 2 years of age are instructed to consult a physician. The product is for external use only and should not be used on larger quantities, particularly over raw surfaces or blistered areas. If the condition worsens or symptoms persist for more than 7 days, the user is advised to discontinue use and contact a doctor. The product should be kept out of reach of children. The inactive ingredients listed include Millegolum (Yarrow) Extract, Capryy| Giycol, GitricAcd, and more. The manufacturer of the product is A.TS. Laboratories, located in Deerfield Beach, FL.*
FDA Label Image

4oz Label (4oz Label)

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