Extra Strength Liquid Numbing Gel
Product Images NDC 69804-022

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Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Extra Strength Liquid Numbing Gel (NDC 69804-022). 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 Slime)

Package Label (2 Oz Slime)
This is a drug fact for a professional use only Lidocaine HCL 4% topical anesthetic. It is used to relieve pain and should be applied to the affected area as needed. The product contains Aloe Vera, Witch Hazel, Organic Alcohol, Kava Kava, Yarrow, Nutmeg, Copaiba Balsam, and Flax Seed Extract as inactive ingredients. The user should test the skin prior to the procedure to check for sensitivity. If sensitivity occurs, the product should be discontinued. The product should not be used on the face, and should be kept out of the reach of children. If the user's skin becomes irritated, worsens or symptoms last longer than 7 days, he/she should contact a doctor. The website for more information is www.naturallyhl.com. The product should be shaken well before each use.*
FDA Label Image

Dosage And Administration (Directions)

Dosage And Administration (Directions)
This text provides directions for using a product on the skin prior to a medical procedure. It advises testing the skin for sensitivity before use and applying the product generously for pain relief. The user should discontinue use if any sensitivity occurs. The product is not suitable for use on the face.*
FDA Label Image

Active Ingredients Section (Act Ing)

Active Ingredients Section (Act Ing)
This is a product that contains Lidocaine Hydrochloride (HCL) 4% as its active ingredient. Lidocaine HCL is a local anesthetic commonly used to numb the skin or mucous membranes before certain medical procedures or surgeries. It is also used to relieve pain or discomfort associated with certain conditions.*
FDA Label Image

Inactive Ingredients Section (Inactive Ingredients)

Inactive Ingredients Section (Inactive Ingredients)
This is a list of inactive ingredients that might be used 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 Section (Indications And Usage)

Indications And Usage Section (Indications And Usage)
This text suggests that the product or medication is designed to provide temporary relief from pain. However, without additional context, it is impossible to determine what specific type of pain the product is designed to treat or how it should be used.*
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 that indicates the product should be kept away from children and should only be used externally. It also advises to avoid contact with the eyes.*
FDA Label Image

Otc Purpose Section (Purpose)

Otc Purpose Section (Purpose)
This product is a topical anesthetic.*
FDA Label Image

Warnings Section (Warning)

Warnings Section (Warning)
This is a warning label that cautions to keep a certain substance out of the reach of children and only use it externally. It also advises 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.