Suave Roll On Powder Antiperspirant Gel
Product Images NDC 83711-146

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Suave Roll On Powder Antiperspirant (NDC 83711-146). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Suave Brands Co, Llc, 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

Powder Roll On Deo Front Label (68455148 Mech Suave Powder Roll On Fop Label 2 7oz V0 Page 0001 (1))

Powder Roll On Deo Front Label (68455148 Mech Suave Powder Roll On Fop Label 2 7oz V0 Page 0001 (1))
Label for Suave Roll on Powder Antiperspirant deodorant gel, showing the Suave logo and the words "Powder roll-on antiperspirant deodorant." The label size is approximately 1.638 inches wide by 1.683 inches high and indicates a net weight of 2.7 oz (80 g). The design features a blue and pink color scheme with decorative swirls. The label was created by CCL Label and includes mechanical artwork identification details.*
FDA Label Image

Men Powder Roll On Antiperspirant Deodorant (70007593 Lbl B Sv Ap Rollon 2.7oz Powder Pp Sg7)

Men Powder Roll On Antiperspirant Deodorant (70007593 Lbl B Sv Ap Rollon 2.7oz Powder Pp Sg7)
Label artwork for Suave Roll on Powder Antiperspirant in a 2.7 oz gel roll-on format. The label includes Drug Facts with active ingredient Aluminum Chlorohydrate (17.6%), directions, warnings, and contact information. It also displays claims such as 24-hour protection and cruelty-free. Packaging dimensions are approximately 1.638 inches by 1.683 inches. The label is produced by Suave Brands Co, LLC and includes a barcode.*

* 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.