Extra Strength Naturally Hl Sunburn Relief
Product Images NDC 69804-041

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 Naturally Hl Sunburn Relief (NDC 69804-041). 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 meant for professional use only to relieve pain temporarily. It contains Lidocaine as an active ingredient and other ingredients like Aloe Vera, Witch Hazel, Organic Alcohol, Kava Kava, etc. It should be applied generously to the affected area after testing skin sensitivity. It is not meant for use on the face and should be discontinued immediately if sensitivity occurs. It is important to avoid contact with eyes and keep it out of reach of children. The product is manufactured by Pain Relief Naturally and can be purchased from www.naturallyhl.com. Shake it well before every use. NDC 69804-041-15 is the product code.*
FDA Label Image

Dosage And Adminstration (Directions)

Dosage And Adminstration (Directions)
This text is a set of directions for using a skin numbing product. It advises testing the skin for sensitivity before use and applying the product generously before or during a procedure to alleviate pain. However, it warns that the product should not be used on the face and use should be discontinued if sensitivity occurs.*
FDA Label Image

Active Ingredients (Act Ing)

Active Ingredients (Act Ing)
This product contains Lidocaine Hydrochloride (HCL) at a concentration of 4%, which is an active ingredient commonly used as a local anesthetic. It can be applied topically to provide temporary relief from pain and discomfort in the affected area.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
This is a list of inactive ingredients present in a product. It includes Aloe Vera, Witch Hazel, Organic Alcohol, Kava Kava, Yarrow, Nutmeg, Copaiba Balsam, and Flax Seed Extract.*
FDA Label Image

Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
This text is a very short sentence that explains the possible uses of a product, which is to provide temporary pain relief.*
FDA Label Image

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

Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)
This is a warning message for a product that should be kept out of reach from children and only be used externally. It also advises avoiding contact with the eyes.*
FDA Label Image

Purpose (Purpose)

Purpose (Purpose)
This text indicates that the purpose of the product is a topical anesthetic, which is a numbing agent applied to the skin to relieve pain or discomfort.*
FDA Label Image

Warnings (Warning)

Warnings (Warning)
This is a warning label typically found on personal care or household products. It warns to keep the product out of reach of children and that it is for external use only. It advises to avoid contact with eyes.*

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