Description
Dove Clinical and Sleep Shield Vanilla Dream Underarm Antiperspirant Deodorant
Dove Stick
FDA Label NDC 64942-2577
9 label sections · Submitted to the FDA by Conopco D/b/a Unilever · 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 64942-2577). 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 17%
Otc - Purpose
Antiperspirant
Indications & Usage
•Reduces underarm wetness
•Extra effective
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
Inactive Ingredient
Stearyl Alcohol, C12-15 Alkyl Benzoate, Isopropyl Palmitate, Cyclopentasiloxane, PPG-14 Butyl Ether, Glycine, Hydrogenated Castor Oil, Calcium Chloride, Fragrance (Parfum), Hydroxystearic Acid, Polyethylene, Helianthus Annuus (Sunflower) Seed Oil, Steareth-100, Stearic Acid, Palmitic Acid, Benzyl Alcohol, Citral, Citronellol, Coumarin, Hexyl Cinnamal, Limonene, Linalool
Otc - Questions
Call 1-800-761-3683
* Please review the disclaimer below.
