Dove Powder Finish Dry Serum Antiperspirant - Aluminum Zirconium Tetrachlorohydrex Gly Stick
Dove Powder Finish Dry Serum Antiperspirant
Dove
FDA Label NDC 64942-1612
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 64942-1612). 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 dove powder finish dry serum antiperspirant - aluminum zirconium tetrachlorohydrex gly stick, drug facts, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Drug Facts
Active Ingredients
Aluminum Zirconium Tetrachlorohydrex GLY (12.9 %)
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, Dimethicone Crosspolymer, Caprylyl Methicone, Fragrance (Parfum), Helianthus Annuus (Sunflower) Seed Oil, Cetyl PEG/PPG-10/1 Dimethicone.
Questions?
Call toll-free 1-800-761-3683
Packaging
Dovepowderfinishdryserumap (67553816labelcarton)
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