Active Ingredient
Aluminum Zirconium Tetrachlorohydrex GLY (15.2%)
Dove Antiperspirant
FDA Label NDC 51769-089
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by All Natural Dynamics for the product Dove Antiperspirant (NDC 51769-089). 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 active ingredient, purpose, uses, warnings, · do not use, · ask a doctor before use if you have, · stop use if, · 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
Purpose
anti-perspirant
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.
· 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, Stearyl Alcohol, C12-15 Alkyl Benzoate, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Parfum, Dimethicone, Polyethylene, Helianthus Annuus Seed Oil, Steareth-100, BHT, Alpha-Isomethyl Ionone, Benzyl Benzoate, Benzyl Salicylate, Butylphenyl Methylpropional, Citronellol, Geraniol, Hexyl Cinnamal, Hydroxycitronellal, Linalool
Questions?
Call 1-800-761-3683
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