Suave Antiperspirant Deodorant Powder Blossom Stick
Product Images NDC 83711-140

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 Antiperspirant Deodorant Powder Blossom (NDC 83711-140). 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

Deo Powder Blossom Front (70007351 Lbl F Sv Deo Powder Blossom 1z Reference Pp Sg3 Front Label)

Deo Powder Blossom Front (70007351 Lbl F Sv Deo Powder Blossom 1z Reference Pp Sg3 Front Label)
Packaging label for Suave Antiperspirant Deodorant Powder Blossom stick, 1 oz (28g). The label features the Suave logo, floral imagery, and states it is an antiperspirant deodorant with sweat and odor protection, talc-free formula. The label includes net weight and some ingredient information, produced by Suave Brands Co, LLC.*
FDA Label Image

Deo Powder Blossom (70007352 Lbl B Sv Deo Powder Blossom 1z Pa Sg5 Page 1)

Deo Powder Blossom (70007352 Lbl B Sv Deo Powder Blossom 1z Pa Sg5 Page 1)
The image shows a label design for Suave Antiperspirant Deodorant Powder Blossom, a 15 g/100 g topical antiperspirant deodorant stick by Suave Brands Co, LLC. The label is for a 1 oz product, displaying drug facts including the active ingredient Aluminum Zirconium Tetrachlorohydrex GLY (15%), usage instructions for underarms, warnings, inactive ingredients, a barcode, and manufacturer information. The label has text in black on a white background with a gloss varnish overlay.*

* 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.