Extra Strength Naturally Hl Foot Care
Product Images NDC 69804-027

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 Foot Care (NDC 69804-027). 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

Dosage And Administration (Dosage And Administration)

Dosage And Administration (Dosage And Administration)
This is a set of directions advising to first test skin sensitivity before applying a pain relief product on a specific area. The product should be applied generously on the affected area. However, if sensitivity occurs, it should be discontinued immediately. It also specifies that the product is not intended for use on the face.*
FDA Label Image

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

Otc Keep Out Of Reach Of Children (Otc Keep Out Of Reach Of Children)
This text is a warning message advising to keep a certain item out of reach of children. The item should be used externally only since contact with the eyes must be avoided.*
FDA Label Image

Warnings (Warnings)

Warnings (Warnings)
This text is a warning label for a product. It cautions to keep the product out of reach of children, and that it should only be used externally. Additionally, it advises to avoid contact with the eyes.*
FDA Label Image

Inactive Ingredients Section (Inactive Ingredients Section)

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

Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
This is a concise statement indicating that the product has a temporary pain-relieving effect. No further information is available regarding the product, its form or the type of pain it is meant to alleviate.*
FDA Label Image

Package Label (Label)

Package Label (Label)
This is a topical anesthetic product that temporarily relieves pain. It contains lidocaine HCL 4% and should not be used on the face. If symptoms worsen or last longer than 7 days, users should stop using the product and contact a doctor. Additionally, it should not be used by people with known allergies to any of the ingredients. The inactive ingredients include Water, Witch Hazel, Organic Alcohol, Kava, Yarrow, Nutmeg, Propolis and (BTMS 50 -A Natural Extract of The). The product was manufactured by Pain Relief Naturally and their web link is WWW.NATURALLYHL.COM. Users must discontinue the product if any sensitivity occurs and avoid contact with eyes. This is a FDA registered product and should be kept out of reach of children.*
FDA Label Image

Otc Active Ingredients Section (Otc Active Ingredients Section)

Otc Active Ingredients Section (Otc Active Ingredients Section)
This product contains Lidocaine HCL 4% as its active ingredient. Lidocaine is a local anesthetic that can provide temporary relief from pain and discomfort. It is commonly used in medical procedures, dental work, and skin treatments. This product may also be used for other purposes, as directed by a healthcare professional.*
FDA Label Image

Otc Purpose Section (Otc Purpose Section)

Otc Purpose Section (Otc Purpose Section)
The text is readable and it is a description of a product that is a topical anesthetic.*

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