Extra Strength Skin Repair
Product Images NDC 69804-051

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 Skin Repair (NDC 69804-051). 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.

Product Images & Figures Index

FDA Label Image

Dosage And Administration (Dosage And Administration)

Dosage And Administration (Dosage And Administration)
This is a set of directions for using a skin product. Before using it, a sensitivity test should be performed to avoid negative reactions. The product should be applied generously to the affected area for pain relief but should be discontinued if any sensitivity occurs. However, it is not intended for use on the face.*
FDA Label Image

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

Keep Out Of Reach Of Children (Otc Keep Out Of Reach Of Children)
This is a warning message for a product. It cautions that the product should be kept away from children, and is meant for use externally only. It also advises against contact with the eyes.*
FDA Label Image

Warnings (Warnings)

Warnings (Warnings)
This text is a warning label that advises to keep a product out of reach of children, that the product is for external use only, and that contact with eyes should be avoided.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients Section)

Inactive Ingredients (Inactive Ingredients Section)
This is a list of inactive ingredients found in a product. It includes water, witch hazel, kava kava, organic yarrow, nutmeg, copaiba balsam, and BTMS 50, which is a natural extract.*
FDA Label Image

Indicaitions And Usage (Indications And Usage)

Indicaitions And Usage (Indications And Usage)
Uses: Temporarily relieves pain.*
FDA Label Image

Package Label (Label)

Package Label (Label)
This is a description of a topical anesthetic product for professional use only. It contains lidocaine HCL 4% and is designed to temporarily relieve pain. Before using, the user should test skin to ensure no sensitivity occurs. It's not suitable for use on the face and if any symptoms last longer than 7 days, the user should discontinue use and seek medical attention. If skin becomes irritated, the user should stop use and consult a doctor. The product is FDA registered and its inactive ingredients include water, witch hazel, organic alcohol, kava, yarrow, nutmeg, and propolis (BTMS 350-A). For more information, visit www.naturallyhl.com. Keep out of reach of children and avoid contact with the eyes.*
FDA Label Image

Active Ingredients (Otc Active Ingredients Section)

Active Ingredients (Otc Active Ingredients Section)
This is a description of an active ingredient called Lidocaine HCL 4%. No further information or context is provided.*
FDA Label Image

Purpose (Otc Purpose Section)

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

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