Extra Strength Naturally Hl Itch Relief
Product Images NDC 69804-033

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 Naturally Hl Itch Relief (NDC 69804-033). 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

Daa (Dosage And Administration)

Daa (Dosage And Administration)
This text provides directions for using a pain relief product topically. The user must test their skin for sensitivity before applying it to the affected area. The product should be applied generously as needed for pain but should not be used on the face. If sensitivity occurs, the user should discontinue use.*
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 appears to be a warning label that comes with a product. The text advises the user to keep the product out of reach of children as it is not suitable for them. It further mentions that the product is for external use only, meaning it should not be consumed or ingested. Finally, it recommends avoiding any contact with the eyes which implies that the product may cause irritation or other side effects if it comes in contact with the eyes.*
FDA Label Image

Warnings Section (Warnings)

Warnings Section (Warnings)
This is a warning label that indicates that a certain product should be kept 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 used in a product. Some of the ingredients include water, witch hazel, kava kava, yarrow, nutmeg and copaiba balsam. There is also a mention of BTMS 50, which is a natural extract.*
FDA Label Image

Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
This text is too short to generate a description. It only states that something is used for temporary pain relief. More information is needed.*
FDA Label Image

Package Label (Label)

Package Label (Label)
This is a description for a FDA registered topical anesthetic. It contains Lidocaine HCL 4% and is intended for professional use only. It provides pain relief and should not be used on the face. Users are warned to discontinue use and seek medical attention if sensitivity occurs. The product should not be used for longer than 7 days and should be kept out of reach of children. Contact information is available on the website naturallyhl.com. The inactive ingredients include Water, Witch Hazel, Organic Alcohol, Kava, Yarrow, Nutmeg, Propolis, and (BTMS 50 -A.*
FDA Label Image

Active Ingredients (Otc Active Ingredients Section)

Active Ingredients (Otc Active Ingredients Section)
This text states that the active ingredient in a certain product is Lidocaine HCL 4%. Further information about the product is not available.*
FDA Label Image

Purpose Section (Otc Purpose Section)

Purpose Section (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.