Axe
Product Images NDC 64942-1169

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Axe (NDC 64942-1169). 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

Axe Dry Essence 2.7 Pdp (Axedryessence2pt7pdp)

Axe Dry Essence 2.7 Pdp (Axedryessence2pt7pdp)
This is a drug facts label for a 24-hour anti-perspirant & deodorant invisible solid with the active ingredient aluminum zirconium tetrachlorohydrex GLY (18.2%). The product is meant for external use only and should not be used on broken skin. Users with kidney disease should consult a doctor before use. In case of rash or irritation, the product should be discontinued. The deodorant should be kept out of reach of children and if swallowed, medical help should be sought immediately. The product is applied only underarms, with the cap needing to be replaced after application. The product should not be stored above 46°C.*

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