Extra Strength Wound Care
Product Images NDC 69804-054

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 Wound Care (NDC 69804-054). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ridge Proeprties, 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

Dosage And Administration (Dosage And Administration)

Dosage And Administration (Dosage And Administration)
This is a set of directions for applying a pain relief product. Before using it, you should test a small area of skin for sensitivity. If there's no reaction, you can apply the product generously to the affected area to relieve pain. However, if there is sensitivity, you should discontinue use. Note that this product 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 is a safety warning label. It advises to keep a certain product out of reach of children and to only use it externally. It also warns to avoid contact with the eyes.*
FDA Label Image

Warnings (Warnings)

Warnings (Warnings)
This is a warning label that advises individuals to keep a product out of reach of children, to only use it externally, and to avoid contact with the eyes.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients Section)

Inactive Ingredients (Inactive Ingredients Section)
This is a list of inactive ingredients found in a product. It includes water, witch hazel, kava kava, organic yarrow, nutmeg, copaiba balsam, and BTMS 50 which is a natural extract.*
FDA Label Image

Uses (Indications And Usage)

Uses (Indications And Usage)
This text suggests that a product or medication is being described. The product is intended for temporary pain relief. However, there is not enough information to determine what type of pain the product aims to alleviate or what form it takes.*
FDA Label Image

Package Label (Label)

Package Label (Label)
This is the product information of a FDA Registered Topical Anesthetic containing Lidocaine HCL 4%. It is advised not to use if the person has any known allergy to any of the ingredients. It is recommended to test the skin before use and check if the skin becomes irritated. The product should be applied generously to the affected area and discontinued if sensitivity occurs or symptoms last longer than 7 days. It should not be used on the face. The product is manufactured by Pain Organic Naturally and contains inactive ingredients such as Water, Witch Hazel, Kava, Yarrow, Nutmeg, Propolis, and (BTMS 350 - A). For contact information, you can visit www.naturallyhl.com. It is a pain relief product for professional use only and should be kept away from the reach of children. It is for external use only, and care must be taken to avoid contact with the eyes.*
FDA Label Image

Active Ingredients (Otc Active Ingredients Section)

Active Ingredients (Otc Active Ingredients Section)
This is a description of a product's active ingredients. The product contains 4% of Lidocaine HCL. No further details are available.*
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.