Extra Strength Scar Prevention
Product Images NDC 69804-063

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Extra Strength Scar Prevention (NDC 69804-063). 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.

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Dosage And Administration (Dosage And Administration)

This is a set of directions for using a topical pain reliever. It recommends testing the skin for sensitivity before use and applying generously to the affected area. It also warns to discontinue use if sensitivity occurs and notes that it should not be used on the face.*

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

This text is a warning to take caution and avoid contact with eyes if using a product intended for external use only. It also emphasizes the importance of keeping the product out of reach of children.*

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Warnings (Warnings)

This text is a warning label that is typically found on the packaging of a product. It cautions the user to keep the product out of reach of children, to use it only externally, and to avoid contact with the eyes.*

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Inactive Ingredients (Inactive Ingredients Section)

This is a list of inactive ingredients that are likely used in a product. These include water, witch hazel, kava kava, organic yarrow, nutmeg, copaiba balsam, and BTMS 50. The product and its purpose are not available.*

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Indications And Usage (Indications And Usage)

This text is too brief and lacking context to produce a useful description. It only states that a product or medication is used for temporary pain relief. More information is needed to provide an accurate description.*

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Package Label (Label)

This is a drug facts label of a topical anesthetic which contains Lidocaine HCL 4%. The product is registered by the FDA and should be used only by professionals. It relieves pain temporarily, and it is not intended for use on the face. It should not be used for more than seven days. If any sensitivity occurs or the skin becomes irritated, the user should discontinue use and seek medical attention. The inactive ingredients of this product include Water, Witch Hazel, Organic Alcohol, Kava, Yarrow, Nutmeg, and Propolis. The product is manufactured by Pain Organic. For further information, one may visit naturallyhl.com.*

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Active Ingredients (Otc Active Ingredients Section)

This product contains Lidocaine HCL 4% as its active ingredient. It is not possible to determine the intended use or form of the product with this information alone.*

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Purpose (Otc Purpose Section)

The purpose of the text is to describe a topical anesthetic.*

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