Description
Axe Black Vanilla Orange and Sandalwood Long Lasting Premium Scent Premium Antiperspirant
Axe Stick
FDA Label NDC 64942-2379
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 64942-2379). 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 Sesquichlorohydrate 9.6%
Otc - Purpose
Antiperspirant
Indications & Usage
apply to underarms only
Warnings
For external use only.
• Do not use on broken skin.• Ask a doctor before
use if you have kidney disease. • Stop use if rash or irritation occurs.
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
Cyclopentasiloxane,Stearyl Alcohol,C12-15 Alkyl Benzoate,PPG-14 Butyl Ether,Hydrogenated Castor Oil,Glycine,PEG-8,Fragrance (Parfum), Calcium Chloride,Dimethicone,Polyethylene,Silica,Helianthus Annuus (Sunflower) Seed Oil,Steareth-100,Stearic Acid,BHT,Alpha-Isomethyl Ionone,Citral,Citronellol,Coumarin,Eugenol,Geraniol,Limonene,Linalool
Otc - Questions
call 1-800-761-3683
* Please review the disclaimer below.
