Junel Fe 1.5/30 Kit
Product Images NDC 63187-890

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Junel Fe 1.5/30 (NDC 63187-890). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Norethindrone Acetate Structural Formula (Ceddd4c3 4827 4294 8767 D1e781a1d611 01)

Chemical structure of norethindrone acetate, one of the active ingredients in Junel Fe 1.5/30, a human prescription drug kit containing norethindrone acetate, ethinyl estradiol, and ferrous fumarate.*

FDA Label Image

Ethinyl Estradiol Structural Formula (Ceddd4c3 4827 4294 8767 D1e781a1d611 02)

Chemical structure of the active ingredient ethinyl estradiol, as labeled in the image.*

FDA Label Image

Table Ii (Ceddd4c3 4827 4294 8767 D1e781a1d611 03)

Bar chart showing mortality rates (number of deaths per 100,000 woman years) across four age groups (15-24, 25-34, 35-44, and 45+). The chart compares four groups: ever-users (non-smokers), controls (non-smokers), ever-users (smokers), and controls (smokers), depicted with different shading patterns indicating the mortality differences by smoking status and user/control status.*

FDA Label Image

63187-890-28 (Ceddd4c3 4827 4294 8767 D1e781a1d611 07)

Label for Junel Fe 1.5mg/30mcg kit containing 28 day tablets. The label shows the product name, quantity (1x28 tablets), and manufacturer Teva Pharmaceuticals USA, Inc. It includes a barcode, NDC 63187-890-28, and instructions to see package insert and keep medication out of reach of children. The label also states the product is RX only and mentions storage temperature (20°-25°C).*

* 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.