Active Ingredient
Aluminum Zirconium Trichlorohydrex Glycine 20%
Duradry Am Deodorant And Antiperspirant
FDA Label NDC 69990-315
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Novadore Usa Inc for the product Duradry Am Deodorant And Antiperspirant (NDC 69990-315). 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, keep out of reach of children, directions, 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 perspiration
Warnings
For external use only.
Stop use if rash or irritation occurs.
Do Not Use
On broken skin
Ask A Doctor Before Use
if you have kidney disease
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
Apply to underarms only
Inactive Ingredients
Caprylic/Capric Triglyceride, Caprylyl Glycol, Cetyl Palmitate, Ethylhexylglycerin, Fragrance, Hydrogenated Castor Oil, Isododecane, Maranta Arundinacea (Arrowroot) Root Extract, Neopentyl Glycol Diheptanoate, Salvia Officinalis (Sage) Oil, Sodium Caproyl/Lauroyl Lactylate, Stearyl Alcohol, Triethyl Citrate.
Questions?
Learn more at duradry.com
Dist. by NOVADORE USA, LLC - Miami, FL 33179
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