Suave
Product Images NDC 64942-1037

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Suave (NDC 64942-1037). 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

Suave Clinical Powder Fresh 1.7 Oz (Suaveclinpowderpdp)

This is a description of a clinical strength deodorant that provides 24-hour wetness protection. It contains aluminum zirconium tetrachlorohydrex GLY (20%) as an active ingredient and should only be used externally. The deodorant should not be applied to broken skin, and people with kidney disease should ask their doctor before use. The user should discontinue use if a rash or irritation occurs and should keep the product out of reach of children. The deodorant should also not be stored above 115°F. The deodorant is manufactured in Canada with US materials and distributed by Unilever.*

FDA Label Image

Suaveclinicalpowdercarton (Suaveclinicalpowdercarton)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.