Extra Strength Aftertat Slime
Product Images NDC 69804-020

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 Aftertat Slime (NDC 69804-020). 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

Package Label (2 Oz Slime)

Package Label (2 Oz Slime)
This text is an advertisement for Tattoo Shine available at www.tatbalm.net with FDA registered drug facts. It is a topical anesthetic with extra strength for professional use only, that temporarily relieves pain. The directions mention testing skin sensitivity prior to procedure and apply as needed for the pain. Discontinue if sensitivity occurs and avoid using on the face. It also mentions to consult a doctor if skin irritation occurs, condition worsens, symptoms last longer than 7 days, or the symptoms clear then reoccur within a few days. The product is not suitable for people with any known allergy to any of the ingredients and should be kept out of reach of children. The inactive ingredients include Flax Seed, Water, Organic Alcohol, Aloe Vera, Nutmeg, Copaiba Balsam, Oils of Moringa Olifera, Walnut, Almond, Rosehip, Eucalyptus, and Coconut. It contains added Lidocaine and Chromium Oxide. The text is marketing material and not a description of the product.*
FDA Label Image

Dosage And Administration (Directions)

Dosage And Administration (Directions)
This text provides instructions for using a product that should be tested on the skin for sensitivity before use. The product should be applied generously to the skin before and/or during a procedure to alleviate pain. However, if sensitivity occurs, use of the product should be stopped immediately. It's important to note that this product is not intended for use on the face.*
FDA Label Image

Active Ingredient (Act Ing)

Active Ingredient (Act Ing)
This product contains Lidocaine HCL 4% as its active ingredient. It is not specified what type of product it is or what it is used for.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
This is a list of inactive ingredients found in a product. The ingredients include Flax Seed, Water, Organic Alcohol, Aloe Vera, Nutmeg, Copaiba Balsam, Oils Of Moringa Oliefera, Walnut, Almond, Rosehip, Eucalyptus, Coconut, and a natural green dye called Chromium Oxide.*
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 is a warning label for a product that should be kept out of reach of children and only used externally. It advises to not allow contact with the eyes.*
FDA Label Image

Purpose (Purpose)

Purpose (Purpose)
The purpose of this text is to describe a topical anesthetic.*
FDA Label Image

Indications And Usage (Uses)

Indications And Usage (Uses)
This product is designed to temporarily relieve pain caused by tattoo procedures.*
FDA Label Image

Warnings Section (Warning)

Warnings Section (Warning)
This is a warning label for a product to caution people to keep it away from children, for external use only and to avoid contact with eyes. It does not provide any further details about the product.*

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