Extra Strength Foot Care Liquid Gel
Product Images NDC 69804-029

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 Foot Care Liquid Gel (NDC 69804-029). 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 with active ingredient T V T T for temporary pain relief. It is registered with the FDA and has NDC # 69804-029-15. The product contains Aloe Vera, Witch Hazel, Organic Alcohol, Kava Kava, Flax Seed Extract, Yarrow, Nutmeg, Copaiba Balsam and is manufactured by Pain Relief Naturally. Test skin for sensitivity before use and apply generously to the affected area as needed for pain. Discontinue use if sensitivity occurs and do not use on the face. Seek medical attention if skin irritation or worsening of symptoms persist or if symptoms recur within a few days. It's only for professional use and should be kept out of reach of children. Shake well before each use. For more information, visit WW.NATURALLYHL.COM.*
FDA Label Image

Directions (Directions)

Directions (Directions)
This text provides directions for a skin product. It recommends testing the skin's sensitivity before using the product and applying it generously prior to and/or during a procedure to alleviate pain. However, if sensitivity occurs, the product should be discontinued. It is not intended for use on the face.*
FDA Label Image

Act-ing. (Act Ing)

Act-ing. (Act Ing)
This is a description of an active ingredient which is Lidocaine HCL 4%. It does not provide any information about the product that contains this ingredient or its uses.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
This is a list of inactive ingredients found in a product. It contains 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 suggests that a product or medication is used to provide temporary relief from pain. However, without additional context, it is impossible to determine what type of pain or product is being referred to.*
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 text is a warning label for a product. It indicates that the product should be kept out of reach of children and only be used externally. It also warns to avoid contact with the eyes.*
FDA Label Image

Purpose (Purpose)

Purpose (Purpose)
This text indicates that the purpose of a certain product is to function as a topical anesthetic.*
FDA Label Image

Warning (Warning)

Warning (Warning)
This text contains a standard warning to keep a certain product out of reach of children, indicating that it is meant for external use only and should not be applied to the eyes. It is not describing any specific product or context.*

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