Nystatin Cream
Product Images NDC 0713-0678

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Nystatin (NDC 0713-0678). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cosette Pharmaceuticals, 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

Image Description (Nystat 1)

Chemical structure of the active ingredient Nystatin, showing its complex molecular formula with multiple hydroxyl, methyl, and other functional groups characteristic of this antifungal compound.*

FDA Label Image

Image Description (Nystat 2)

Nystatin Cream, USP topical cream label shows 100,000 units per gram strength in a 15 g tube. The label includes usage instructions, manufacturer Cosette Pharmaceuticals, Inc., and warnings for external use only, not for ophthalmic use. The NDC code 0713-0678-15 and barcode are also visible.*

FDA Label Image

Image Description (Nystat 3)

Nystatin Cream, USP 100,000 units per gram topical cream in a 15 g tube by Cosette Pharmaceuticals, Inc. The label includes dosage instructions, storage conditions, and a barcode. It is marked Rx only and for external use only, not for ophthalmic use.*

FDA Label Image

Image Description (Nystat 4)

Packaging label for Nystatin Cream USP, 100,000 units per gram, in a 30 g tube. The label specifies it is for external use only and not for ophthalmic use. Manufactured by Cosette Pharmaceuticals, Inc. The label includes a barcode, NDC 0713-0678-31, and usage instructions to apply liberally twice daily to affected areas.*

FDA Label Image

Image Description (Nystat 5)

Nystatin Cream, USP 100,000 units per gram topical cream in a 30 g tube. The label is from Cosette Pharmaceuticals, Inc. It includes usage directions, storage instructions, ingredient list, and a barcode. The label states the product is for external use only and not for ophthalmic use, with an NDC of 0713-0678.*

* 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.