Extra Strength Shingle Chickenpox Relief
Product Images NDC 69804-060

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Extra Strength Shingle Chickenpox Relief (NDC 69804-060). 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.

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Dosage And Administration (Dosage And Administration)

This text provides instructions for using a pain relief product. It advises testing the skin for sensitivity before use, applying the product generously to the affected area, and discontinuing use if sensitivity occurs. It also warns that the product should not be used on the face.*

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

This text is a warning label. It cautions that the product should be kept away from children and only used externally. It also warns to avoid contact with the eyes.*

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Warnings (Warnings)

This is a warning message advising to keep a product out of reach of children, use it only for external use, and avoid contact with the eyes. It does not provide any information about the product itself.*

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Inactive Ingredients (Inactive Ingredients Section)

This is a list of inactive ingredients that are likely to be part of a product formulation. It includes various natural extracts, such as Witch Hazel, Kava Kava, Yarrow, and Copaiba Balsam, alongside some other components like water, nutmeg, and BTMS 50.*

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Indications (Indications And Usage)

This is a short text that mentions the use of a product to alleviate pain on a temporary basis. The specific product or pain type is not mentioned.*

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Package Label (Label)

This is a drug fact sheet for a topical anesthetic product. It comes in extra strength and contains Lidocaine HCL 4% as an active ingredient. It should not be used for longer than 7 days or on the face. The manufacturer is Pain Organic Alcohol and more information can be found on their website, www.naturallyhl.com. It is registered with the FDA but should not be used if the user has any known allergies to any of the ingredients. It should be discontinued if sensitivity occurs, and medical attention should be sought if any issues occur. The product is intended for professional use only and should be kept out of reach of children.*

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Active Ingredients (Otc Active Ingredients Section)

This is a description of the active ingredient in a product, which is Lidocaine HCL at a concentration of 4%. No additional information is provided.*

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Purpose (Otc Purpose Section)

This text suggests that the purpose of the product is a Topical Anesthetic.*

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