Active Ingredient:
Aluminum Zirconium Trichlorohydrex Gly 20%
Duradry
FDA Label NDC 58443-0430
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Prime Enterprises Inc. for the product Duradry (NDC 58443-0430). 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:, otc - do not use, otc - ask doctor, otc - keep out of reach of children, otc - stop use, 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.
Otc - Do Not Use
Do not use on broken skin.
Otc - Ask Doctor
Ask a doctor before use if you have kidney disease.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Otc - Stop Use
Stop use if rash or irritation occurs.
Directions:
Apply to underarms only.
Inactive Ingredients:
C13-15 Alkane, Caprylic/Capric Triglyceride, Caprylyl Glycol, Cetyl Palmitate, Ethylhexylglycerin, Fragrance, Hydrogenated Castor Oil, Isododecane, Isohexadecane, Maranta Arundinacea (Arrowroot) Root Extract, Salvia Officinalis (Sage) Oil, Sodium Caproyl/Lauroyl Lactylate, Stearyl Alcohol, Triethyl Citrate
Questions?
Learn more at duradry.com
Duradry Am Deodorant & Antiperspirant Barca - 65 G
Principle Display Label (58443 0430 3)
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