Ban Liquid
Product Images NDC 10596-336

3 FDA label images from Kao Usa Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ban (NDC 10596-336). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kao 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

10596 336 15 Updated

10596 336 15 Updated
Label for Ban Roll-On Antiperspirant Deodorant Regular, showing 1.5 FL OZ (44 mL) liquid roll-on. Active ingredient is Aluminum chlorohydrate 18%, used as an antiperspirant. Label includes drug facts covering uses, warnings, directions for applying underarms only, storage information, and lists inactive ingredients. Labeler is Kao USA Inc.*
FDA Label Image

10596 336 35 Updated

10596 336 35 Updated
Label for Ban Roll-On Antiperspirant Deodorant Regular with active ingredient Aluminum Chlorohydrate 18%, in a 3.5 FL OZ (103 mL) liquid topical dosage form. The label highlights features like cruelty-free, paraben-free, and dye-free. The product is made by Kao USA Inc. and includes a drug facts panel with usage, warnings, directions, and inactive ingredients.*
FDA Label Image

10596 336 70 Updated

10596 336 70 Updated
The image shows the packaging label for Ban Roll-On Antiperspirant Deodorant Regular containing 2 units, each with 3.5 fl oz (103 mL) of liquid. It contains Aluminum Chlorohydrate 20 g per 103 mL as the active ingredient. The label includes usage directions, warnings, company contact information, and certification logos. The product is distributed by Kao USA Inc.*

* 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.