Progesterone Liquid
Product Images NDC 43742-0851

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Progesterone (NDC 43742-0851). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Deseret Biologicals, Inc., 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

Progesterone (Dsrt59 Progesterone 2 7 24)

Label for Progesterone homeopathic liquid oral solution, 1 FL OZ (30 ml), by Deseret Biologicals, Inc. Identifies active ingredient Progesterone with multiple potencies and lists inactive ingredients as demineralized water and 25% ethanol. The label includes Drug Facts covering uses, warnings, directions, and other information, along with the NDC 43742-0851-1 and contact details for the distributor.*

* 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.