Antiperspirant Above Extreme Sun Men Aerosol, Spray
Product Images NDC 73306-1162

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 Antiperspirant Above Extreme Sun Men (NDC 73306-1162). 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 Aerossois 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

0981e559 D8c7 C87f E063 6294a90a7af1

0981e559 D8c7 C87f E063 6294a90a7af1
Packaging label for ABOVE EXTREME SUN MEN antiperspirant aerosol spray, 19 mg/90 g, by Baston Industria de Aerossóis Ltda. The orange label highlights 72-hour dry and lasting protection, with usage and warnings in Portuguese, Spanish, and English. The label lists ingredients including aluminum sesquichlorohydrate, and displays flammable and cruelty-free symbols. Net content is 150 ml/90 g.*
FDA Label Image

Label (Antitranspirante Above Extreme Sun 150ml (1))

Label (Antitranspirante Above Extreme Sun 150ml (1))
ANTIPERSPIRANT ABOVE EXTREME SUN MEN aerosol spray label with strength 19 mg/90g. The label features bright orange, yellow, and blue colors with the brand name ABOVE EXTREME prominently displayed. It includes usage instructions and drug facts in English, Spanish, and Portuguese. The product offers 72-hour dry and lasting protection, is made by Baston Industria de Aerossois Ltda, and contains aluminum sesquichlorohydrate as the active ingredient. The container size is 150 ml/90 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.