Description
Axe Phoenix 48H Sweat and Odor Protection Antiperspirant Deodorant Stick
Axe Stick
FDA Label NDC 64942-2399
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Conopco D/b/a Unilever for the product Axe (NDC 64942-2399). 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 description, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Aluminum Zirconium Tetrachlorohydrex GLY 18.2%
Otc - Purpose
Antiperspirant
Indications & Usage
reduces underarm wetness
Warnings
For external use only.
Do not use on broken skin.
Stop use if rash or irritation occurs.
Ask a doctor beforeuse if you have kidney disease.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed,get medical help or contact a Poison Control Center right away.
Dosage & Administration
apply to underarms only
Inactive Ingredient
PPG-14 Butyl Ether,Cyclopentasiloxane,Stearyl Alcohol,Isopropyl Palmitate,Mineral Oil,Hydrogenated Castor Oil,PEG-8 Distearate,Fragrance (Parfum),Polyethylene,BHT,Alpha-Isomethyl Ionone,Cinnamal, Coumarin,Eugenol,Hexyl Cinnamal,Limonene,Linalool
Otc - Questions
Call toll-free 1-800-450-7580
* Please review the disclaimer below.
