Progesterone Capsule
Product Images NDC 51655-542

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Progesterone (NDC 51655-542). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

51655-542-26 (51655 542 26 Rev A 05 23)

51655-542-26 (51655 542 26   Rev A 05 23)
Label for Progesterone Capsules 100 mg by Northwind Health Company, LLC. The label indicates 90 capsules per container, prescription only. Storage instructions specify controlled room temperature 20°-25°C (68°-77°F). Additional warnings include keeping out of reach of children and avoiding use if allergic to peanuts. The label also includes NDC 51655-542 and lot and expiration placeholders.*
FDA Label Image

Figure 1 (Progesterone Fig1)

Figure 1 (Progesterone Fig1)
A line graph showing probability of hyperplasia over time (months) on medication up to 36 months. It compares three treatment groups: Conjugated Estrogens Alone, Conjugated Estrogens Plus Micronized Progesterone (cyclical), and Placebo Only. The graph includes patient numbers at each time point and depicts increasing hyperplasia probability with conjugated estrogens alone compared to the other two groups.*
FDA Label Image

Chemical Structure (Progesterone Str)

Chemical Structure (Progesterone Str)
Chemical structure of progesterone, a steroid hormone compound, showing fused ring systems with ketone groups and methyl substituents, consistent with its known molecular framework.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.