Dove
Product Images NDC 64942-1204

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 (NDC 64942-1204). 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 Clinical Cleartone 1.7 Oz Pdp (Doveclinicalprotectcleartonepdp)

Dove Clinical Cleartone 1.7 Oz Pdp (Doveclinicalprotectcleartonepdp)
Drug Facts panel of Dove Clinical Protection Cleartone Antiperspirant and Deodorant. It lists the active ingredient as Aluminum Zirconium Tetrachlorohydrex GLY (20%) as an antiperspirant. The panel provides uses, warnings, directions for application, other information including storage instructions, and inactive ingredients. Contact information for questions and distributor details for Unilever are also included.*
FDA Label Image

Dove Clinical Cleartone 1.7 Oz Carton (Doveclinicalprotectcleartonecarton)

Dove Clinical Cleartone 1.7 Oz Carton (Doveclinicalprotectcleartonecarton)
Packaging label for Dove Clinical Protection Cleartone Antiperspirant and Deodorant. The label shows the brand name Dove and highlights the clinical protection with prescription strength wetness protection. It features ClearTone to help restore skin to its natural tone and mentions dermatologist testing. The net weight is 1.7 oz (48g). The label includes active ingredient information, usage directions, drug facts, and a satisfaction guarantee from Conopco Inc. d/b/a Unilever.*

* 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.