Nystatin Powder
Product Images NDC 68382-370

4 FDA label images from Zydus Pharmaceuticals Usa Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nystatin (NDC 68382-370). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Pharmaceuticals Usa 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

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Chemical structure of nystatin, the active ingredient in NYSTATIN powder topical formulation by Zydus Pharmaceuticals USA Inc.*
FDA Label Image

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The label for Nystatin Topical Powder, USP displays nystatin concentration as 100,000 units per gram in a 15-gram container. It is labeled for topical use only and produced by Cadila Healthcare Ltd., distributed by Zydus Pharmaceuticals (USA) Inc. The label includes storage instructions, dosage guidance for topical application, and a barcode with the NDC 68382-370-01.*
FDA Label Image

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Label for Nystatin Topical Powder, USP, containing 100,000 units per gram for topical use only. The label indicates a 30 gram size, manufactured by Cadila Healthcare Ltd. and distributed by Zydus Pharmaceuticals (USA) Inc. Storage and usage instructions are provided, along with the NDC 68382-370-02.*
FDA Label Image

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Label for Nystatin Topical Powder, USP containing 100,000 units per gram, intended for topical use only. The package contains 60 grams and is labeled for prescription use. Manufactured by Cadila Healthcare Ltd., India, and distributed by Zydus Pharmaceuticals USA Inc. Storage instructions and usage warnings are also visible.*

* 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.