Otc - Active Ingredient
Active Ingredient
Aluminum Zirconium Tetrachlorohydrex GLY (15.2%)
Dove
FDA Label NDC 64942-1349
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 64942-1349). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - ask doctor, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
anti-perspirant
Indications & Usage
Uses
reduces underarm wetness
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
Inactive Ingredient
Inactive ingredients
Cyclopentasiloxane, Stearyl Alcohol, C12-15 Alkyl Benzoate, PPG-14 Butyl Ether, Hydrogenated Castor Oil, PEG-8, Dimethicone, Fragrance (Parfum), Silica, Polyethylene, Helianthus Annuus (Sunflower) Seed Oil, Steareth-100, BHT, Butyrospermum Parkii (Shea) Butter, Hydroxyethyl Urea
Otc - Questions
Questions?
Call 1-800-761-3683
Packaging
Doveacsheabutterpdp (1349)
* Please review the disclaimer below.
