Extra Strength Pretat
Product Images NDC 69804-018

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Extra Strength Pretat (NDC 69804-018). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ridge Properties, 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

Dosage And Administration (Dosage And Administration)

Dosage And Administration (Dosage And Administration)
This text contains instructions for using a skin test product, advising the user to discontinue use if any sensitivity occurs. It suggests applying thick layers every 3-5 minutes until the desired level of pain relief is achieved, but warns not to use the product near the eyes.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients Section)

FDA Label Image

Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
The text suggests that the product or solution it refers to is intended to help individuals manage or alleviate pain that may be associated with tattoos. It may be a temporary solution that offers some level of relief to the user.*
FDA Label Image

Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)

Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)
This text appears to be a warning about a product. It suggests that if the product is ingested, one should seek medical help or contact a poison control center immediately. The product is not specified in the text.*
FDA Label Image

Active Ingredients (Otc Active Ingredient)

Active Ingredients (Otc   Active Ingredient)
This is a description for a product or medication that contains Lidocaine Hydrochloride (HCL) as its active ingredient with a concentration of 4%. Lidocaine is a local anesthetic that can be used for numbing the skin or mucous membranes to alleviate pain or discomfort caused by medical procedures or skin conditions.*
FDA Label Image

Principal Display Panel (Principal Display Panel)

Principal Display Panel (Principal Display Panel)
This is a FDA registered drug with NDC# 69804-018-12. The drug contains Lidocaine HCL 4% and other inactive ingredients. This drug shouldn't be used if a person has any known allergy. It is only for professional use and not suitable for use around the eyes. In case of ingestion or any serious allergic reaction, medical attention is necessary. The product is manufactured, packed, and distributed by Pain Relief Naturally, and it is available in 4 ounces of gel. Prior to use, the skin should be tested for sensitivity. If the skin becomes irritated, use should be stopped and seek the help of a doctor. It is recommended not to use the drug on or near the eyes.*
FDA Label Image

Purpose (Purpose)

Purpose (Purpose)
This is a description of a product that is being used as a topical anesthetic.*
FDA Label Image

Warnings Section (Warnings Section)

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