Extra Strength Postpartum Relief
Product Images NDC 69804-042

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Extra Strength Postpartum Relief (NDC 69804-042). 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)

This text provides directions for using a pain-relieving product on the skin. Prior to use, a sensitivity test is recommended. The product should be applied generously to the affected area, and use should be discontinued if any sensitivity occurs. This product is not meant for use 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 message that advises people to keep a certain product away from children. It is intended for external use only, meaning that it should not be ingested or used internally. Additionally, it cautions against getting the product into the eyes.*

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Warnings (Warnings)

This text is a warning label for a product, reminding users to keep it out of reach of children, use it only on external surfaces, and to avoid contact with the eyes.*

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Inactive Ingredients Section (Inactive Ingredients Section)

This is a list of inactive ingredients used in a product. The ingredients include Water, Witch Hazel, Kava kava, Organic Yarrow, Nutmeg, Copaiba Balsam, and BTMS 50.*

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Indications And Usage (Indications And Usage)

This text suggests that a specific product or medication can provide temporary relief from pain. However, without additional information such as the name of the product, the type of pain it treats, or the duration of the pain relief, it is difficult to provide further details.*

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Package Label (Label)

This is a product with Lidocaine HCL 4% as the active ingredient, which is registered by the FDA to relieve pain. The product should not be used on the face and should not be used for longer than seven days. If skin irritation occurs, discontinue use and seek medical attention. There is a list of inactive ingredients, and for more information, you can visit the website. It is a topical anesthetic for professional use only, and you should avoid contact with the eyes. Keep out of reach of children.*

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Active Ingredients (Otc Active Ingredients Section)

This is a product that contains Lidocaine Hydrochloride (HCL) as its active ingredient in a concentration of 4%. Further information about the product is not provided.*

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Otc 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.