FDA Label for Axe Night Antiperspirant And Deodorant
View Indications, Usage & Precautions
Axe Night Antiperspirant And 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.
Axe Night Antiperspirant And Deodorant - Aluminum Zirconium Tetrachlorohydrex Gly Stick
Axe Night Antiperspirant and Deodorant
Drug Facts
Active ingredient
Aluminum Zirconium Tetrachlorohydrex GLY (11.4 %)
Purpose
antiperspirant
Uses
• reduces underarm wetness
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.
Directions
apply to underarms only
Inactive Ingredients
Cyclopentasiloxane, PPG-14 Butyl Ether, Stearyl Alcohol, Polyethylene, Hydrogenated Castor Oil, PEG-8 Distearate, Fragrance (Parfum), Silica, BHT.
Questions?
Call toll-free 1-800-450-7580
Packaging
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