Active Ingredient
Aluminum Zirconium Octachlorohydrex GLY 16.4%
Dry Idea Antiperspirant
FDA Label NDC 54340-290
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Henkel Corporation for the product Dry Idea Antiperspirant (NDC 54340-290). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, stop use and ask a doctor, keep out of reach of children., ask a doctor before use if, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiperspirant
Use
• Reduces underarm perspiration • Extra effective
Warnings
For external use only.Do not use on broken skin.
Stop Use And Ask A Doctor
if rash or irritation occurs.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a poison control center right away.
Ask A Doctor Before Use If
you have kidney disease.
Directions
Apply to underarms only.
Inactive Ingredients
Aqua (Water, Eau) • Alcohol Denat. • Cyclomethicone • Propylene Glycol • Dimethicone • Calcium Chloride • Trisiloxane • PEG/PPG-18/18 Dimethicone • Hexamethylindanopyran • Dipropylene Glycol • T-Butyl Alcohol
Storage And Handling
Do not freeze or store above 105°F.
Otc - Questions
Questions? 1-800-258-DIAL
* Please review the disclaimer below.
