Giselle Antiperspirant Deodorant Roll-on For Women Cream
Product Images NDC 84178-011

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 Giselle Antiperspirant Deodorant Roll-on For Women (NDC 84178-011). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Evi Labs, 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

Giselle Back Render (Giselle Back Render)

Giselle Back Render (Giselle Back Render)
Drug Facts panel on a roll-on deodorant showing aluminum chlorohydrate 10% as the active ingredient for antiperspirant use. Includes warnings for external use only, not applying on broken skin, and contacting a doctor if kidney disease is present. Directions advise shaking well and applying to underarms only. Lists inactive ingredients and distributor contact information.*
FDA Label Image

Giselle From Render (Giselle From Render)

Giselle From Render (Giselle From Render)
GISELLE Antiperspirant Deodorant Roll-On for Women in cream form with a white container and a pink cap. The label displays the brand name GISELLE and indicates it is a long-lasting fragrance version. The net weight is 3 oz. The product is labeled by EVI LABS.*
FDA Label Image

Giselle Panel (Giselle Panel)

Giselle Panel (Giselle Panel)
Drug Facts panel from GISELLE Antiperspirant Deodorant Roll-On for Women cream. Lists active ingredient aluminum chlorohydrate 10% as antiperspirant, usage information, warnings, directions, and inactive ingredients. Distributed by Zermat USA Inc. with contact information and barcode shown.*

* 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.