Dry Idea Advanced Dry Antiperspirant And Deodorant Clear Gel Unscented Gel
Product Images NDC 82699-101

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 Dry Idea Advanced Dry Antiperspirant And Deodorant Clear Gel Unscented (NDC 82699-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Thriving Brands Llc, 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

Warnings (1327463 Back Label)

Warnings (1327463 Back Label)
Drug Facts panel for Dry Idea Advanced Dry Antiperspirant and Deodorant Clear Gel Unscented. Lists Aluminum Zirconium Octachlorohydrex GLY 16.4% as the active ingredient and states its use to reduce underarm perspiration. Includes warnings for external use only, to avoid broken skin, and to consult a doctor if rash or irritation occurs or if kidney disease is present. Directions specify application to underarms only. Inactive ingredients and storage instructions are also provided.*
FDA Label Image

Package Label Principal Display Panel (1327463 Front Label)

Package Label Principal Display Panel (1327463 Front Label)
Packaging label for Dry Idea Advanced Dry Antiperspirant and Deodorant Clear Gel Unscented. The label highlights it as hypoallergenic, goes on clear, and offers extra effective odor protection for up to 72 hours. The net weight is 3 oz (85 g). The product is an antiperspirant and deodorant gel.*

* 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.