FDA Label for Axe Clinical Protection Antiperspirant And Deodorant
View Indications, Usage & Precautions
Axe Clinical Protection 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.
Otc - Active Ingredient
Active Ingredient Purpose
Aluminum Zirconium Tetrachlorohydrex GLY (20%).................anti-perspirant
Warnings
Warnings For External Use only
Inactive Ingredient
Cyclopentasiloxane, Dimethicone, Microcrystalline Wax, C18-36 Acid Triglyceride, Fragrance (Parfum), Silica, Dimethicone Crosspolymer, BHT.
Otc - Questions
Questions? Call toll-free 1-800-450-7580
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.
Package Label.Principal Display Panel
PDP 1.7oz
Outer Carton PDP 1.7 oz
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