Studio 35 Beauty
Product Images NDC 0363-2013

View Photos of 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 Studio 35 Beauty (NDC 0363-2013). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Walgreen Company, 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

Studio (Studio)

Studio (Studio)
Studio 35 Beauty Clinical Strength Deodorant packaging label from Walgreen Company, NDC 0363-2013, features powder fresh scent. The antiperspirant/deodorant contains aluminum zirconium trichlorohydrex gly as the active ingredient and offers maximum strength protection against wetness. The net weight is 1.6 OZ (45 g). Directions, drug facts, and inactive ingredients are included on the label.*
FDA Label Image

Label Back (Studioback)

Label Back (Studioback)
Drug Facts panel for studio 35 beauty Clinical Strength antiperspirant. Lists aluminum zirconium trichlorohydrex gly 20% as the active ingredient and its purpose. Includes use instructions, warnings, directions for application, and inactive ingredients. States distribution by Walgreen Co. with contact details. Claims 100% satisfaction guarantee.*
FDA Label Image

Label Front (Studiofront)

Label Front (Studiofront)
Label of studio 35 beauty Clinical Strength deodorant by WALGREEN COMPANY. It features a pink and white design with text indicating clinical strength deodorant, powder fresh scent, maximum strength protection against wetness, and aluminum zirconium trichlorohydrex gly as the active ingredient. Net weight is 1.6 oz (45 g).*

* 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.