FDA.reportPublic FDA data

Duradry Antiperspirant Deodorant Stick

Manufacturer
NOVADORE USA Inc
Effective date
2025-11-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:43:18

Label at a glance#

ProductDuradry Antiperspirant Deodorant Stick
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure11 sections

Indications and uses

Reduces underarm perspiration

Dosage and administration

Apply to underarms only

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Trichlorohydrex Glycine 20%

Purpose

OTC - PURPOSE SECTION

​Antiperspirant

Uses

INDICATIONS & USAGE SECTION

Reduces underarm perspiration

Warnings

WARNINGS SECTION

For external use only.

Stop use if rash or irritation occurs.

Do not use

OTC - DO NOT USE SECTION

On broken skin

Ask a doctor before use

OTC - ASK DOCTOR SECTION

if you have kidney disease

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 Antiperspirant Deodorant Stick (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYCINE)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Clear SkyClear Sky

LimitlessLimitless

BarcaBarca

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130860002304069GTIN-13: 0860002304069
EAN-13: 0860002304069
GTIN-12: 860002304069
UPC-A: 860002304069
GTIN storage (14 digits): 00860002304069		Clear Sky.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69990-316-01Duradry Antiperspirant Deodorant Stick65 g in 1 CYLINDERSTICK651
69990-316-01Duradry Antiperspirant Deodorant Stick1 in 1 CYLINDERSTICK11

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69990-31669990-316-01

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
STEARYL ALCOHOL2KR89I4H1YIACT
MARANTA ARUNDINACEA ROOTFVN346W31AIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
TRIETHYL CITRATE8Z96QXD6UMIACT
ISODODECANEA8289P68Y2IACT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB
C13-15 ALKANE114P5I43UJIACT
FRAGRANCE 135765EM498GW35IACT
ISOHEXADECANE918X1OUF1EIACT
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDEFJ1H6M2JG9IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
SALVIA OFFICINALIS ROOT236QY0A1BLIACT
SODIUM CAPROYL LACTYLATE87WR3BHC09IACT
CETYL PALMITATE5ZA2S6B08XIACT
CAPRYLYL GLYCOL00YIU5438UIACT

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
Duradry Antiperspirant Deodorant StickALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYCINENOVADORE USA Inc43556d04-53c6-15e1-e063-6294a90a0c462025-11-11WarningsExact identifier
ndc (package): 69990-316-01
ndc (product): 69990-316
ndc11 (package): 69990031601
spl id: 43556c05-69ed-1276-e063-6294a90a968e
spl set id: 43556d04-53c6-15e1-e063-6294a90a0c46

Reported adverse events (FAERS/openFDA)#

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