FDA Label for Axe Signature Island Antiperspirant Deodorant
View Indications, Usage & Precautions
Axe Signature Island Antiperspirant Deodorant Product Label
The following document was submitted to the FDA by the labeler of this product Conopco Inc. D/b/a Unilever. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Active ingredient
Aluminum Zirconium Tetrachlorohydrex GLY(15.2%)
Otc - Purpose
Purpose
antiperspirant
Indications & Usage
Uses
· reduces underarm wetness
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 have kidney disease
Otc - Stop Use
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
Directions
apply to underarms only
Inactive Ingredient
Inactive Ingredients Cyclopentasiloxane, Stearyl Alcohol, C12-15 Alkyl Benzoate, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Fragrance (Parfum), Dimethicone, Polyethylene, Helianthus Annuus (Sunflower) Seed Oil, Steareth-100, BHT.
Otc - Questions
Questions?
Call toll-free 1-800-450-7580
2.7 Oz Pdp
* Please review the disclaimer below.