Miconazole Nitrate Cream
Product Images NDC 51672-2070

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Miconazole Nitrate (NDC 51672-2070). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Figure (Miconazole 01)

An instructional illustration showing two steps for handling a cream tube: the first step depicts twisting off the safety seal from the tube tip, and the second step shows removing the screw-on cap. This image likely relates to the use or preparation of a vaginal cream product.*

FDA Label Image

Figure (Miconazole 02)

An instructional line drawing illustrating a hand opening a tube by peeling back a protective seal or tab from the tube's opening. This is likely an instruction step for preparing to use a topical cream, such as Miconazole Nitrate vaginal cream.*

FDA Label Image

Figure (Miconazole 03)

An instructional line drawing illustrating the use of a vaginal cream applicator. The image shows a hand holding the applicator, labeling the plunger and barrel components typically used to administer miconazole nitrate vaginal cream.*

FDA Label Image

Figure (Miconazole 04)

Biomedical illustration showing the female pelvic anatomy related to vaginal medication application. Labels identify the urinary opening, vagina, rectum, cervix, and uterus. A hand is shown inserting a vaginal applicator, illustrating the proper anatomical placement for medication delivery.*

FDA Label Image

Principal Display Panel (25 g Tube Carton)

Packaging label for Miconazole 3 Miconazole Nitrate Vaginal Cream USP (4%), a vaginal antifungal cream indicated as a 3-day treatment. The label highlights 3 disposable applicators and a tamper-evident seal warning. Distributed by Taro Pharmaceuticals U.S.A., indicating a 0.9 oz (25 g) tube included in the package.*

* 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.