Extra Strength Postherpetic Neuralgia Care
Product Images NDC 69804-057

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 Postherpetic Neuralgia Care (NDC 69804-057). 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

Dosage And Administration (Dosage And Administration)

Dosage And Administration (Dosage And Administration)
This text appears to be a product instruction or warning label about a topical pain reliever. It advises testing the skin prior to use and suggests applying the product generously to the affected area as needed for pain. However, users should discontinue use if any allergic reaction or sensitivity occurs, and it should not be used on the face.*
FDA Label Image

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

Keep Out Of Reach Of Children (Otc Keep Out Of Reach Of Children)
This text is a warning that advises people to keep a product out of reach from children, use it only for external purposes, and avoid eye contact.*
FDA Label Image

Warnings (Warnings)

Warnings (Warnings)
This is a warning message intended for parents and guardians to keep a product out of reach of children. The product is meant for external use only and it is advised to avoid any contact with the eyes.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients Section)

Inactive Ingredients (Inactive Ingredients Section)
This is a list of inactive ingredients present in a product. The ingredients are water, Witch Hazel, Kava kava, Organic Yarrow, Nutmeg, Copaiba Balsam, and BTMS 50 (a natural extract).*
FDA Label Image

Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
This is a short text that highlights that a product or medication provides temporary pain relief. Unfortunately, there is not enough context to identify the specific brand, type or use case for this product.*
FDA Label Image

Package Label (Label)

Package Label (Label)
This is a drug label for a topical anesthetic product that contains 4% Lidocaine HCL. It is used to temporarily relieve pain, but should not be applied to the face or used on anyone with a sensitivity to its ingredients. The product is not for professional use only, but care should be taken to avoid contact with the eyes, and it should be kept out of the reach of children. Inactive ingredients include water, witch hazel, organic alcohol, kava, yarrow, nutmeg, propolis, and BTMS 350-A. If skin irritation persists or worsens after 7 days of using the product, or if symptoms clear up and then reoccur within a few days, the user is advised to stop using it and contact a doctor. More information can be obtained at www.naturallyhl.com.*
FDA Label Image

Active Ingredients (Otc Active Ingredients Section)

Active Ingredients (Otc Active Ingredients Section)
This product contains the active ingredient Lidocaine HCL 4%.*
FDA Label Image

Purpose (Otc Purpose Section)

Purpose (Otc Purpose Section)
Purpose: Topical Anesthetic.*

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