Dove Ultimate Go Fresh Refreshing
Product Images NDC 64942-1052

2 FDA label images from Conopco Inc. D/b/a Unilever · 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 Dove Ultimate Go Fresh Refreshing (NDC 64942-1052). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Conopco Inc. D/b/a Unilever, 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

Dove Ugf Refreshing 2.6 Oz Back Pdp (Doveugfrefreshing2pt6backpdp)

Dove Ugf Refreshing 2.6 Oz Back Pdp (Doveugfrefreshing2pt6backpdp)
Drug Facts panel for Dove Ultimate Go Fresh Refreshing Antiperspirant and Deodorant listing active ingredient as Aluminum Zirconium Tetrachlorohydrex GLY (14.8%) as an antiperspirant. It states uses including reducing underarm wetness and providing 24-hour protection. Warnings include external use only, avoiding use on broken skin, and consulting a doctor if there is kidney disease. Directions specify applying to underarms only. It also includes other information about storage temperature and lists inactive ingredients. Manufacturer contact information for Conopco Inc. d/b/a Unilever in Trumbull, CT is provided.*
FDA Label Image

Dove Ugf Refreshing 2.6 Oz Front Pdp (Doveugfrefreshing2pt6frontpdp)

Dove Ugf Refreshing 2.6 Oz Front Pdp (Doveugfrefreshing2pt6frontpdp)
Label for Dove Ultimate Go Fresh Refreshing Antiperspirant and Deodorant by Conopco Inc. d/b/a Unilever. The label features the Dove logo and branding, mentions a waterlily and freshmint scent, and includes the net weight of 2.6 oz (74 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.