Antiperspirant Towlette
Product Images NDC 55726-200

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Antiperspirant Towlette (NDC 55726-200). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zero Sweat, 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

Inner Label (Zero Sweat Antiperspirant Inner Label)

This is a user instruction for using the ZeroSweat antiperspirant towelette to keep armpits dry. It recommends drying armpits before use and dabbing on the antiperspirant rather than rubbing. The product may cause a tingling sensation after application, which is normal. In case of irritation, users can apply an anti-itch cream. The active ingredient is Aluminum Chloride 14%. The product is not to be sold separately and is distributed by ZeroSweat Inc in Clearfield, Utah. For more information, visit ZeroSweat.com.*

FDA Label Image

Outer Label (Zero Sweat Antiperspirant Outer Label)

This is a drug facts label for an antiperspirant containing Aluminum Chloride 14%. It's intended use is to reduce underarm perspiration. The product is only for external use, not to be used on broken skin, and should be stopped if any rash or irritation occurs. Individuals with kidney disease should ask a doctor before use. It contains several inactive ingredients such as water, polysorbate 20, and sage leaf extract. Additionally, the label promotes an antiperspirant towelette called ZeroSweat, which claims to provide up to 7 days of protection from sweat and is intended to be used at bedtime, for people who suffer from excessive sweating.*

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