Extra Strength Postpartum Relief
Product Images NDC 69804-044

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 Postpartum Relief (NDC 69804-044). 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

Package Label (2 Oz)

Package Label (2 Oz)
This is a description of a topical anesthetic with active ingredients listed as "| 0 Y111 T 5 (O DR U728". It is registered with the FDA and has an NDC number of 69804-044-15. The product is manufactured by Pain Relief Naturally and has inactive ingredients including Aloe Vera, Witch Hazel, Organic Alcohol, Kava Kava, Yarrow, Nutmeg, Copaiba Balsam, and Flax Seed Extract. The product is used to temporarily relieve pain, but it should not be applied to the face. Prior to use, the skin should be tested, and if sensitivity occurs or symptoms worsen or last longer than seven days, it should be discontinued, and a doctor should be consulted. Children should not have access to the product, and it is meant for external use only.*
FDA Label Image

Dosage And Administration (Directions)

Dosage And Administration (Directions)
This text provides directions for using a pain-relieving product on the skin during a medical or cosmetic procedure. It is recommended to test the skin for sensitivity before use and to apply the product as needed for pain relief. However, if sensitivity occurs, the use of the product should be discontinued. It is important to note that this product should not be used on the face.*
FDA Label Image

Active Ingredients (Act Ing)

Active Ingredients (Act Ing)
This is a description of a product that contains Lidocaine HCL 4% as its active ingredient. Without further context, it is not possible to determine what type of product it is or what it is used for.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
This is a list of inactive ingredients found in a product. It contains a mixture of natural ingredients such as Aloe Vera, Witch Hazel, Kava Kava, Yarrow, Nutmeg, Copaiba Balsam, and Flax Seed Extract, as well as Organic Alcohol. It is unclear what the product is or its purpose.*
FDA Label Image

Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
This is a very short and simple text stating that the given product is used to provide temporary relief from pain. No details about the type of pain or the product itself are provided.*
FDA Label Image

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

Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)
This text provides a warning for a product to keep out of reach of children, and that it should only be used externally. It also advises avoiding contact with the eyes.*
FDA Label Image

Purpose (Purpose)

Purpose (Purpose)
Purpose: Topical Anesthetic.*
FDA Label Image

Warnings (Warning)

Warnings (Warning)
This is a warning label for a product advising to keep it out of reach of children and only use it externally. It also mentions to avoid contact with eyes.*

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