Extra Strength Pretat
Product Images NDC 69804-002

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Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Extra Strength Pretat (NDC 69804-002). 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 is a set of directions for a pain relief product. It advises the user to test the product on their skin before using it, and to discontinue use if any sensitivity occurs. The product should be applied in thick, even layers every 3-5 minutes until the desired level of pain relief is achieved. However, the user should avoid using this product near their eyes.*
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Inactive Ingredients (Inactive Ingredients Section)

Inactive Ingredients (Inactive Ingredients Section)
This is a list of inactive ingredients present in a product. The ingredients are propylene glycol, water, and Kava. The text also includes some codes and symbols, as well as the names of some other compounds, such as dimethicone/divinyldimethicone/silsesquioxane crosspolymer and benzyl alcohol.*
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Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
This text suggests that a certain product is used for providing temporary relief from pain caused by a tattoo.*
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Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)

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Active Ingredient (Otc Active Ingredient)

Active Ingredient (Otc   Active Ingredient)
This product contains 4% Lidocaine HCL, an active ingredient commonly used for its numbing properties. It may be used in various medical and cosmetic procedures as a local anesthetic.*
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Principal Display Panel (Principal Display Panel)

Principal Display Panel (Principal Display Panel)
This is a product called TAT Balm that is registered by the FDA and contains Lidocaine HCL 4% as an active ingredient. This product should not be used near the eyes, and individuals with known allergies to the ingredients should not use it. The product is intended for professional use only, and consumers are advised to seek medical attention if an adverse reaction occurs. The directions suggest testing the skin for sensitivity prior to use and applying thick layers every 3-5 minutes until the desired level of pain relief is achieved. The product should be discontinued if skin irritation occurs. The inactive ingredients include propylene glycol, water, Kava, avocado oil, copaiba balsam, ceteryl alcohol, and polyacrylate among others. The product is manufactured, packed, and distributed by Pain Relief Naturally, and consumers can contact them in case of a serious adverse reaction. TAT Balm is intended for a pleasurable tattoo experience.*
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Purpose (Purpose)

Purpose (Purpose)
Purpose: Topical Anesthetic.*
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Warnings Section (Warnings Section)

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