Extra Strength Liquid Insect Bite Relief Gel
Product Images NDC 69804-025

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 Insect Bite Relief Gel (NDC 69804-025). 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.

Product Images & Figures Index

FDA Label Image

Package Label (2 Oz)

Package Label (2 Oz)
This is a topical anesthetic gel containing Lidocaine HCL 4%, which provides relief from pain. The active ingredient is FDA registered with National Drug Code (NDC) # 69804-025-15. It is advised to test the skin's sensitivity before application and discontinue use if the skin becomes irritated. The product is not recommended for use on the face. If symptoms last longer than 7 days or if they reoccur within a few days, discontinue use, and consult a doctor. The product contains active ingredients like Aloe Vera, Witch Hazel, organic alcohol, Kava Kava, and flaxseed extract. For contact info and manufacturing details, visit naturallyhl.com. Keep out of reach of children and avoid contact with eyes.*
FDA Label Image

Dosage And Adminstration (Directions)

Dosage And Adminstration (Directions)
This text provides instructions for using a product on the skin during a procedure to alleviate pain. It advises testing for sensitivity before application and discontinuing use if any sensitivity occurs. Additionally, it specifies that the product is not intended for use on the face.*
FDA Label Image

Otc Active Ingredients Section (Act Ing)

Otc Active Ingredients Section (Act Ing)
This is a medication with lidocaine HCL 4% as its active ingredient. However, without additional information, it is not possible to determine its purpose or use.*
FDA Label Image

Inactive Ingredients Section (Inactive Ingredients)

Inactive Ingredients Section (Inactive Ingredients)
This text appears to be a list of inactive ingredients in a product, possibly a topical solution or supplement. The ingredients include Aloe Vera, Witch Hazel, Organic Alcohol, Kava Kava, Yarrow, Nutmeg, Copaiba Balsam, and Flax Seed Extract. It is possible that these ingredients were intentionally chosen for their beneficial properties or their ability to support the main active ingredient of the product.*
FDA Label Image

Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
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 a warning label for a product advising people to keep it away from children and avoid contact with eyes. It is meant for external use only.*
FDA Label Image

Otc Purpose (Purpose)

Otc Purpose (Purpose)
The provided text says "Purpose: Topical Anesthetic". This is a brief description indicating that the product is a topical anesthetic, which means it is meant to numb or relieve pain on the skin's surface.*
FDA Label Image

Warnings Section (Warning)

Warnings Section (Warning)
This text provides a warning to keep a product out of reach of children, as it is for external use only. Additionally, it advises avoiding contact with the eyes.*

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