Anti-fungal Powder Miconazole Nitrate Powder
Product Images NDC 56104-500

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Anti-fungal Powder Miconazole Nitrate (NDC 56104-500). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Premier Brands Of America 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 1 (Endzone Antifungal Powder 50 081ez 51 081ez)

Image 1 (Endzone Antifungal Powder 50 081ez 51 081ez)
This text provides information about an antifungal powder containing Miconazole Nitrate 2%. The powder is used to treat most cases of athlete's foot, jock itch, and ringworm. It absorbs moisture and relieves itching, burning, scaling, and chafing. The product is talc-free and is for external use only. It should not be used on children under 2 years old without the guidance of a doctor and should be kept away from the eyes. If irritation occurs or there is no improvement within a certain timeframe (4 weeks for athlete's foot and ringworm, 2 weeks for jock itch), it is recommended to stop using the product and consult a doctor. The directions include cleaning the affected area and applying a thin layer of the powder twice daily. The powder is not effective on the scalp or nails. The product contains inactive ingredients such as allantoin, chloroxylenol, fragrance, and microcrystalline cellulose. It is manufactured in the USA and distributed by Premier Brands of America Inc. For any questions or concerns, a phone number is provided.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.