Antitranspirante Above Maxx Original Cream
Product Images NDC 73306-1190

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 Antitranspirante Above Maxx Original (NDC 73306-1190). 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

4f462a64 4416 95b3 E063 6394a90af96a

4f462a64 4416 95b3 E063 6394a90af96a
Packaging label for ANTITRANSPIRANTE ABOVE MAXX ORIGINAL cream, a topical antiperspirant for women. The label indicates a content volume of 250 mL (150 g), featuring moisturizing action and 72-hour antiperspirant effectiveness. The product is alcohol-free with no residue. Labeler is BASTON INDUSTRIA DE AEROSSOIS LTDA. The label includes directions, ingredients, warnings, and multilingual text.*
FDA Label Image

Above Cream Original Woman Antiperspirant Deodorant 72h (Antitranspirante Above Maxx Cream Original)

Above Cream Original Woman Antiperspirant Deodorant 72h (Antitranspirante Above Maxx Cream Original)
Packaging label for ANTITRANSPIRANTE ABOVE MAXX ORIGINAL cream, topical antiperspirant for women. The label states a quantity of 250 ml / 150 g (8.4 fl oz / 5.3 oz) and highlights moisturizing action, 72-hour antiperspirant effect, no residue, and alcohol-free formulation. The product is labeled by Baston Industria de Aerossois Ltda and includes safety and usage information in Spanish and Portuguese.*

* 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.