Extra Strength Pretat
Product Images NDC 69804-019

8 FDA label images from Ridge Properties · 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 69804-019). 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)
Directions panel for Extra Strength PreTAT, stating to test skin for sensitivity before use and discontinue if sensitivity occurs. It instructs to apply thick even layers every 3-5 minutes until the desired level of pain relief is reached and warns not to use near the eyes.*
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Inactive Ingredients (Inactive Ingredients Section)

Inactive Ingredients (Inactive Ingredients Section)
Text panel listing the inactive ingredients of Extra Strength PreTAT. Ingredients include Propylene Glycol, Water, Kava Kava, Copaiba Balsam, Acrylates C10-30 Alkyl Acrylate Crosspolymer, and Benzyl Alcohol. The text is red on a black background with 'Inactive Ingredients:' in bold.*
FDA Label Image

Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
A text panel highlighting a single usage indication: "For temporary relief of tattoo pain." The text uses red font on a black background with the words "Uses -" in bold followed by the italicized description.*
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Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)

Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)
A warning text panel in red uppercase letters on a black background advises to keep the product out of reach of children, use it only externally, avoid use around the eyes, and seek medical help or poison control immediately if ingested.*
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Active Ingredient (Otc Active Ingredient)

Active Ingredient (Otc   Active Ingredient)
A text panel titled 'Active Ingredient' displaying the active ingredient Lidocaine HCL at a strength of 4%. The text is styled with 'Active Ingredient:' in large red font and 'Lidocaine HCL - 4%' in italicized red font on a black background.*
FDA Label Image

Principal Display Panel (Principal Display Panel)

Principal Display Panel (Principal Display Panel)
The label for Extra Strength PreTAT by Ridge Properties displays the product name prominently in large red letters on a black background. It indicates the product is a 3.4 oz gel designed for easy application in tattoo numbing with 1% lidocaine. The label includes usage directions, warnings, active and inactive ingredients, and a barcode. The active ingredient is Lidocaine HCl at 4%, and inactive ingredients include propylene glycol, water, Kava Kava, Copaiba Balsam, and others. Ridge Properties is the labeler, with the NDC 69804-019.*
FDA Label Image

Purpose (Purpose)

Purpose (Purpose)
A text panel prominently displaying the purpose of the product labeled as "Topical Anesthetic" in red italicized font on a black background.*
FDA Label Image

Warnings (Warnings Section)

Warnings (Warnings Section)
Warning text panel from Extra Strength PreTAT by ridge properties. It includes safety warnings about keeping the product out of reach of children, external use only, not for use around eyes, and instructions to seek medical help if ingested. It also advises stopping use and consulting a doctor if skin irritation or worsening symptoms occur or symptoms last longer than 7 days or return after clearing.*

* 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.