Extra Strength Liquid Hemorrhoid Relief Gel
Product Images NDC 69804-024

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 Liquid Hemorrhoid Relief Gel (NDC 69804-024). 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 Slime)

Package Label (2 Oz Slime)
This is a drug facts label for a topical anesthetic containing Lidocaine HCL 4%, indicated for relieving pain. It comes with directions to test skin sensitivity prior to use, apply generously as needed for pain, and discontinue use if sensitivity occurs. Not for use on the face. Further, it informs that if the skin becomes irritated, the condition worsens or any symptoms last longer than 7 days, or the symptoms clears up then reoccur within a few days, a doctor should be consulted. The label also includes various warnings such as keeping the product out of reach of children, avoiding contact with eyes, and seeking medical attention if any adverse effects occur. The product is manufactured by Pain Relief Naturally, and for contact information, visit their website. Shake well before each use. You can pick some more at WWW.NATURALLYHL.COM.*
FDA Label Image

Dosage And Sdministration (Directions)

Dosage And Sdministration (Directions)
This is a set of directions for using a skin product before and during a procedure. The user is advised to test their skin for sensitivity before use and apply the product generously as needed for pain relief during the procedure. However, if sensitivity occurs, the user is advised to discontinue use of the product. It is also mentioned that the product is not suitable for use on the face.*
FDA Label Image

Otc Active Ingredients (Act Ing)

Otc Active Ingredients (Act Ing)
This text indicates that the active ingredient of the substance being referred to is Lidocaine hydrochloride (HCL) and its concentration is 4%. It is likely used as an anesthetic or pain reliever.*
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Inactive Ingredients Section (Inactive Ingredients)

Inactive Ingredients Section (Inactive Ingredients)
This is a list of inactive ingredients found in a product. Some of the ingredients are Aloe Vera, Witch Hazel, Organic Alcohol, Kava Kava, Yarrow, Nutmeg, Copaiba Balsam, and Flax Seed Extract. It is unclear what the product is and how these ingredients are used within it.*
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Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
This text provides brief information about the use of a product that can relieve pain for a short period of time. It does not provide any details about the product name, specific type of pain it can relieve or any possible side effects.*
FDA Label Image

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

Otc Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)
This is the warning label of a product that needs to be kept away from children and only for external use. It also cautions to avoid contact with the eyes.*
FDA Label Image

Purpose Section (Purpose)

Purpose Section (Purpose)
Purpose: Topical Anesthetic.*
FDA Label Image

Warnings Sections (Warning)

Warnings Sections (Warning)
This is a warning label that indicates a product should be kept out of reach of children and only used externally. It also warns to avoid contact with the eyes.*

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