Antiperspirant Above Dolce Vita Aerosol, Spray
Product Images NDC 73306-1107

2 FDA label images from Baston Industria De Aeross�is Ltda · 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 Antiperspirant Above Dolce Vita (NDC 73306-1107). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baston Industria De Aeross�is Ltda, 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

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Antiperspirant Above Dolce Vita 48h aerosol spray in a 150 ml / 90 g container. The label features the brand name Above Women and Dolce Vita in stylized fonts with an anti-perspirante claim. It highlights that the product is dry spray, triclosan-free, and alcohol-free. The active ingredient is Aluminum Sesquichlorohydrate (24%). Manufactured by Baston Industria de Aerossóis Ltda, made in Brazil, and distributed by Spray International LLC, Medley Florida.*
FDA Label Image

Package Label (Antitranspirante Above Dolce Vita 150ml)

Package Label (Antitranspirante Above Dolce Vita 150ml)
Label for Antiperspirant Above Dolce Vita 24g/100g aerosol spray for women, manufactured by Baston Industria de Aerossóis Ltda. The design features a purple and red color scheme with 'Dolce Vita 48h Antitranspirante' prominently displayed. The net content is 150ml/90g (5.07 fl. oz / 3.17 oz). The active ingredient listed is Aluminum Sesquichlorohydrate. The label includes drug facts, warnings, directions, and cosmetic ingredients in multiple languages, along with flammable warnings and contact information for the manufacturer and distributor.*

* 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.