Extra Strength Sunburn Relief
Product Images NDC 69804-039

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Extra Strength Sunburn Relief (NDC 69804-039). 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 text provides directions for using a topical pain reliever, advising the user to test the skin for sensitivity before applying it to the affected area as needed. It also warns the user to discontinue use if sensitivity occurs and notes that the product 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 label typically found on products that need to be kept away from children. It advises that the product is only intended for external use and must not come into contact with the eyes.*

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Warnings (Warnings)

This is a warning label for a product that should be kept out of reach of children. It is meant for external use only, and should not come into contact with the eyes.*

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Inactive Ingredients (Inactive Ingredients Section)

This text lists the inactive ingredients present in a product. These include water, witch hazel, kava kava, organic yarrow, nutmeg, copaiba balsam, and BTMS 50, which is a natural extract.*

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Indications And Usage (Indications And Usage)

This text is too short to provide any context or details. It appears to be a fragment of a sentence related to pain relief. Based on this fragment, it can be inferred that it refers to a product or medication that is used for temporarily relieving pain. However, without more context, it is impossible to provide a useful description.*

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Package Label (Label)

This is a description of a FDA registered topical anesthetic product. The product label warns the users not to use it if they have an allergy to any of its ingredients. It provides NDC# 69804-039-02 to identify it. The active ingredient is Lidocaine HCL 4%. It is not intended to be used on the face and should be discontinued if sensitivity occurs or if it lasts for over 7 days. The product is manufactured by Pain Organic and the company's contact information can be found at WWW.NATURALLYHL.COM. The product is made using Water, Witch Hazel, Organic Alcohol, Kava, Yarrow, Nutmeg, and Propolis as inactive ingredients.*

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Active Ingredients (Otc Active Ingredients Section)

This is a description of a product's active ingredients. The product contains Lidocaine HCL 4%. No further information regarding the product is available.*

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Purpose Section (Otc Purpose Section)

This product is a topical anesthetic.*

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