Drug Facts
Active ingredient
Aluminum Sesquichlorohydrate (12.15 %)
Dove Stick
FDA Label NDC 64942-1925
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 Inc. D/b/a/ Unilever for the product Dove (NDC 64942-1925). 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 drug facts, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, questions?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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 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
Water (Aqua), Cyclopentasiloxane, C12-15 Alkyl Benzoate, Synthetic Wax, Glycerin, Calcium Chloride, Cetyl PEG/PPG-10/1 Dimethicone, Glycine, Fragrance (Parfum), Helianthus Annuus (Sunflower) Seed Oil, Alpha-Isomethyl Ionone, Benzyl Alcohol, Benzyl Benzoate, Benzyl Salicylate, Coumarin, Hexyl Cinnamal, Limonene, Linalool
Questions?
Call toll-free 1-800-761-3683
Packaging
Dove Men Ultimate Coastal Cedar Ap Deo Is (Dovemencoastalcedarapdeois)
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