Extra Strength Skin Repair
Product Images NDC 69804-048

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 69804-048). 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 provides directions for using a pain relief product on the affected area of the skin, but recommends testing for skin sensitivity prior to use. It also states that the product should not be used on the face and should be discontinued if sensitivity occurs.*
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 text is a cautionary statement indicating that a product should be kept away from children, used only externally, and that contact with eyes should be avoided. It is likely a warning label for a cosmetic or cleaning product.*
FDA Label Image

Warnings (Warnings)

Warnings (Warnings)
This text is a warning label for a product, indicating that it should be kept away from children, it is for external use only, and should not come into contact with the eyes.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients Section)

Inactive Ingredients (Inactive Ingredients Section)
This is a list of inactive ingredients that may be used 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

Indications (Indications And Usage)

Indications (Indications And Usage)
Uses: Temporarily relieves pain.*
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Package Label (Label)

Package Label (Label)
This is a description of a topical anesthetic with lidocaine HCL 4% as the active ingredient. The product is FDA registered, but users should test the skin for any allergies before use. It should not be used continuously for more than seven days, and if symptoms worsen or persist, a doctor should be consulted. The product has been manufactured by Pain Organic Naturally and contains inactive ingredients such as water, witch hazel, kava, yarrow, nutmeg, and Propolis. It is primarily intended for professional use to relieve pain and should not be used on the face, and caution should be taken while using this product around children. For more details about the product or contact information, visit the website, www.naturallyhl.com.*
FDA Label Image

Active Ingredients (Otc Active Ingredients Section)

Active Ingredients (Otc Active Ingredients Section)
This text is a list of active ingredients, specifically mentioning Lidocaine HCL 4%. It may be found on a label or packaging of a product.*
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.