Extra Strength Liquid Burn Relief Gel
Product Images NDC 69804-026

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 Liquid Burn Relief Gel (NDC 69804-026). 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)

Package Label (2 Oz)
This is a topical anesthetic with active ingredients for pain relief. It should be applied to the affected area after testing skin sensitivity. Discontinue use if sensitivity occurs and do not use on face. Consult a doctor if the skin becomes irritated or condition worsens. It temporarily relieves pain and is for professional use only. Keep out of reach of children and avoid contact with the eyes. Other ingredients include Aloe Vera, Witch Hazel, and Nutmeg. For more information and contact details, visit WW.NATURALLYHL.COM.*
FDA Label Image

Dosage And Administration (Directions)

Dosage And Administration (Directions)
This text is a set of directions for using a pain-relieving product on the skin during a procedure. Before use, a sensitivity test should be carried out on the skin. The product can be applied generously to the skin before and/or during the procedure as necessary for pain relief. If sensitivity occurs, use should be discontinued, and the product should not be used on the face.*
FDA Label Image

Otc Active Ingredients Section (Act Ing)

Otc Active Ingredients Section (Act Ing)
This is a description of an active ingredient, specifically Lidocaine HCL 4%. No additional information is provided.*
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Inactive Ingredients Section (Inactive Ingredients)

Inactive Ingredients Section (Inactive Ingredients)
This is a list of inactive ingredients found in a product or medication. It includes Aloe Vera, Witch Hazel, Organic Alcohol, Kava Kava, Yarrow, Nutmeg, Copaiba Balsam, and Flax Seed Extract. This information may be relevant for individuals who are sensitive or allergic to any of these ingredients.*
FDA Label Image

Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
This text suggests that a product is being described that has pain relief properties which are temporary in nature. However, more information is necessary to understand the specifics of the product, such as its name and its method of application.*
FDA Label Image

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

Otc Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)
This text is a warning about a product that should be kept out of the reach of children and used only externally. It also advises avoiding contact with the eyes.*
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Otc Purpose Section (Purpose)

Otc Purpose Section (Purpose)
Purpose: Topical Anesthetic.*
FDA Label Image

Warnings Section (Warning)

Warnings Section (Warning)
This text provides a warning label for a product, indicating that it should be kept out of children's reach and should only be used externally. The text also states that contact with the eyes should be avoided.*

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