Description
Dove Advanced Care Revive Antiperspirant Deodorant
Dove Stick
FDA Label NDC 64942-2529
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 D/b/a Unilever for the product Dove (NDC 64942-2529). 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 description, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Aluminum Sesquichlorohydrate 12.8%
Otc - Purpose
Antiperspirant
Indications & Usage
• reduces underarm wetness
• 72 Hour Protection
Warnings
• For external use only.
• Do not use on broken skin. •
Stop use if rash or irritation occurs. •
Ask a doctor before use if you have kidney disease. • If swallowed, get medical help or contact a Poison Control Center right away.
Otc - Keep Out Of Reach Of Children
• KEEP OUT OF REACH OF CHILDREN.
Dosage & Administration
•Apply to underarms only
•Turn dial to raise product
•Apply a thin layer to underarms
• Replace cap
•To ensure product appears clear on skin, do not overapply
Inactive Ingredient
Cyclopentasiloxane, Stearyl Alcohol, C12-15 Alkyl
Benzoate, PPG-14 Butyl Ether, Hydrogenated
Castor Oil, Glycine, PEG-8, Calcium Chloride,
Dimethicone, Silica, Hydroxystearic Acid,
Polyethylene, Fragrance (Parfum), Helianthus
Annuus (Sunflower) Seed Oil, Steareth-100,
Stearic Acid, BHT, Benzyl Alcohol, Citronellol,
Coumarin, Limonene, Linalool
Otc - Questions
Call 1-800-761-3683
* Please review the disclaimer below.
