Otc - Active Ingredient
Active ingredient
Aluminum Zirconium Tetrachlorohydrex GLY(18.2%)
Axe Stick
FDA Label NDC 64942-2352
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 Inc. D/b/a Unilever for the product Axe (NDC 64942-2352). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - ask doctor, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purposeanti-perspirant
Indications & Usage
Uses
·reduces underarm wetness
·24 hour protection
Warnings
Warnings
For external use only
Otc - Do Not Use
Do not use on broken skin
Otc - Ask Doctor
Ask a doctor before use if you havekidney disease
Otc - Stop Use
Stop useif 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
Directions
·
apply to underarms only
·turn dial to raise product
·to ensure product appears clear on skin, do not overapply
·replace cap
Inactive Ingredient
Inactive ingredients
Cyclopentasiloxane, PPG-14 Butyl Ether, Stearyl Alcohol, Hydrogenated Castor Oil, PEG-8 Distearate, Talc, Fragrance (Parfum), BHT.
Otc - Questions
Questions?
Call toll-free 1-800-450-7580
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