Norgestimate And Ethinyl Estradiol Kit
Product Images NDC 42291-590

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Norgestimate And Ethinyl Estradiol (NDC 42291-590). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avkare, 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

Inner (590 28 Inner Carton)

This is a medication information card providing details such as dosage, tablet count, lot number, and expiration date. The text is relatively difficult to read as it includes errors and is not properly formatted.*

FDA Label Image

Large (591 84 Large Carton)

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Blister (Blister Pack)

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Chart 1

Not available.*

FDA Label Image

Ethinyl (Ethinyl Estradiol)

Etinyl Estradiol is a medication used in hormonal birth control pills, patches, and vaginal rings to prevent pregnancy. It is a synthetic form of estrogen and works by preventing ovulation, thickening cervical mucus to prevent sperm from reaching the egg, and thinning the lining of the uterus to make it harder for a fertilized egg to attach and grow. It is typically used in combination with other hormones, such as progestin.*

FDA Label Image

Figure 2

The text provides a figure and a table with data from different studies on the risk of breast cancer associated with the use of combined oral contraceptives in women. The studies are from different countries and years. The estimates of effects are given in terms of relative risk (RR), odds ratio (OR), or hazard ratio (HR). The text provides definitions for the terms "ever COC use" and "never COC use."*

FDA Label Image

Norgestimate (Norgestimate)

* 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.