FDA Label for Dove Clinical Protection Powder Soft Antiperspirant And Deodorant
View Indications, Usage & Precautions
Dove Clinical Protection Powder Soft 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
Aluminum Zirconium Tetrachlorohydrex GLY (20%)
Otc - Purpose
Purpose
anti-perspirant
Indications & Usage
Uses
• reduces underarm wetness
• extra effective
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
• before bed, apply two clicks of product to each underarm
Inactive Ingredient
Inactive ingredients
Cyclopentasiloxane, Dimethicone, Paraffin, Microcrystalline Wax, Silica, Fragrance (Parfum), Helianthus Annuus (Sunflower) Seed Oil, Dimethicone Crosspolymer, BHT.
Otc - Questions
Questions? Call toll-free 1-800-761-3683
1.7 Oz Pdp
1.7 Oz Carton
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