Fraicheur The Vert Antiperspirant And Deodorant Roll-on
Product Images NDC 54235-207

2 FDA label images from Yves Rocher North America Inc. Dba Laboratoire De Biologie Vegetal Yves Rocher · 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 Fraicheur The Vert Antiperspirant And Deodorant Roll-on (NDC 54235-207). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Yves Rocher North America Inc. Dba Laboratoire De Biologie Vegetal Yves Rocher, 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

Back Label (Fraicheur The Vert Antiperspirant And Deodorant Roll On Back Label)

Back Label (Fraicheur The Vert Antiperspirant And Deodorant Roll On Back Label)
Drug Facts panel for FRAICHEUR THE VERT ANTIPERSPIRANT AND DEODORANT ROLL-ON. Lists aluminum sesquichlorohydrate 15% as the active ingredient for use as an antiperspirant to reduce underarm perspiration. Includes warnings for external use, directions to apply as needed, and a list of non-medicinal ingredients such as water, cyclopentasiloxane, and camellia sinensis leaf extract. Also contains manufacturer and distributor information from Yves Rocher North America Inc.*
FDA Label Image

Front Label (Fraicheur The Vert Antiperspirant And Deodorant Roll On Front Label)

Front Label (Fraicheur The Vert Antiperspirant And Deodorant Roll On Front Label)
Label of FRAICHEUR THE VERT antiperspirant and deodorant roll-on by Yves Rocher North America Inc. It shows a green tea leaf illustration and states the product volume as 60 ml (2.0 fl. oz.). The label includes product identification in English, French, and Spanish.*

* 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.