Ban Liquid
Product Images NDC 10596-338

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ban (NDC 10596-338). 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 338 15 Updated

Ban Roll-On Antiperspirant Deodorant Unscented 1.5 FL OZ (44 mL) in an invisible roll-on liquid dosage form by Kao USA Inc. The label highlights aluminum chlorohydrate 18% as the active ingredient to reduce underarm perspiration. The image includes the front label, Drug Facts panels with warnings, directions, and inactive ingredients, and a barcode with contact information.*

FDA Label Image

10596 338 35 Udpated

Packaging label for Ban Roll-On Antiperspirant Deodorant Unscented containing 3.5 FL OZ (103 mL) of liquid. The front displays the brand name Ban, indicates it is unscented, invisible roll-on, cruelty-free, paraben free, dye free, and an antiperspirant deodorant. The back label includes Drug Facts listing Aluminum Chlorohydrate 18% as the active antiperspirant ingredient, directions for use, warnings, inactive ingredients, and contact information for Kao USA Inc.*

FDA Label Image

10596 338 70 Updated

Ban Roll-On Antiperspirant Deodorant Unscented 20 g/103 mL liquid topical product packaging label. The box features pink and green colors with drug facts panel stating active ingredient Aluminum Chlorohydrate 20%. The label includes use, warnings, directions, inactive ingredients, and contact information. Labeled as a value pack with 2x protection, made by Kao USA Inc., and bearing sustainability and recycling logos.*

* 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.