FDA.reportPublic FDA data

Duradry

Manufacturer
Prime Enterprises, Inc.
Effective date
2022-02-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:09:36

Label at a glance#

ProductDuradry Antiperspirant Deoderant
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure8 sections

Indications and uses

Reduces underarm perspiration

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Trichlorohydrex Gly 20%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

Reduces underarm perspiration

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on broken skin.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

kidney disease.

Stop use

OTC - STOP USE SECTION

if rash or irritation occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

Learn more at duradry.com

Duradry AM Deoderant & Antiperspirant Barça

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principle Display LabelPrinciple Display Label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58443-053358443-0533-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
C13-15 ALKANE114P5I43UJIACT
SODIUM CAPROYL LACTYLATE87WR3BHC09IACT
CAPRYLYL GLYCOL00YIU5438UIACT
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
ISODODECANEA8289P68Y2IACT
MARANTA ARUNDINACEA ROOTFVN346W31AIACT
SAGE OILU27K0H1H2OIACT
STEARYL ALCOHOL2KR89I4H1YIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CETYL PALMITATE5ZA2S6B08XIACT
TRIETHYL CITRATE8Z96QXD6UMIACT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
ISOHEXADECANE918X1OUF1EIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d733eea0-13ef-73da-e053-2995a90aad4bb851fe5c-d8f6-12da-e053-2a95a90a86f92022-02-04WarningsExact identifier
spl id: d733eea0-13ef-73da-e053-2995a90aad4b
spl set id: b851fe5c-d8f6-12da-e053-2a95a90a86f9

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.