Defense Antifungal Medicated Bar Soap
Product Images NDC 70856-3581

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Defense Antifungal Medicated Bar (NDC 70856-3581). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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FDA Label Image

31 01034756 Approval Defense Antifungal Tinted 4.2oz

31 01034756 Approval Defense Antifungal Tinted 4.2oz
This is a drug information for an antifungal cream containing tolnaftate 1.0% which is clinically effective in treating athlete's foot, ringworm, and jock itch. It relieves itching, burning, and cracking skin. The cream should not be used on children under 2 years except under the advice and supervision of a doctor. It should not come in contact with the eyes. If there is no improvement after 2 weeks of use for jock itch or 4 weeks for athlete's foot and ringworm, a doctor should be consulted. The cream should be used 1-2 times a day for 4 weeks for athlete's foot, paying special attention to the spaces between toes and wearing well-fitting ventilated shoes. The product is not effective on the scalp or nails. Inactive ingredients include Sodium Palmate, Sodium Palm Kernelate, Water, Glycerin, Sodium Gluconate, Eucalyptus Globulus Leaf Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Palm Acid, Sodium Chloride, Palm Kernel Acid, Charcoal Powder.*

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