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

8 FDA label images from Ridge Properties · 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)
Drug Facts panel for extra strength foot care liquid gel by Ridge Properties with NDC 69804-029. Lists active ingredient Lidocaine HCL 4% as a topical anesthetic. Details uses for temporary pain relief, warnings to keep out of reach of children, and directions to test skin sensitivity. Includes inactive ingredients and advises discontinuation if irritation occurs. Contains a barcode and a logo with the text 'Naturally HL'.*
FDA Label Image

Directions (Directions)

Directions (Directions)
Directions text panel for extra strength foot care liquid gel by Ridge Properties instructing to test skin sensitivity before use, apply generously to skin prior to or during procedure as needed for pain, discontinue if sensitivity occurs, and warning not to use on the face.*
FDA Label Image

Act-ing. (Act Ing)

Act-ing. (Act Ing)
This image shows the active ingredients section of a drug facts panel, highlighting Lidocaine HCL at a concentration of 4%. It appears to be part of the labeling information for a topical product.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
Text panel listing inactive ingredients of the product extra strength foot care liquid gel by Ridge Properties. The inactive ingredients are 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)
Drug facts text panel showing the 'Uses' section, stating that the product temporarily relieves pain. The text is white on a black background.*
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)
A black warning label with white text stating: Keep out of reach of children, for external use only, and avoid contact with the eyes.*
FDA Label Image

Purpose (Purpose)

Purpose (Purpose)
A text panel section labeled 'Purpose:' identifies the product's purpose as a Topical Anesthetic. The text is white on a black background with 'Purpose:' italicized and 'Topical Anesthetic' in bold font.*
FDA Label Image

Warning (Warning)

Warning (Warning)
Warning text panel stating: Keep out of reach of children, for external use only, and avoid contact with the eyes.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.