FDA.reportPublic FDA data

Duradry AM Deodorant and Antiperspirant

Manufacturer
NOVADORE USA Inc
Effective date
2023-11-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:59:55

Label at a glance#

ProductDuradry AM Deodorant and Antiperspirant
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

Dist. by NOVADORE USA, LLC - Miami, FL 33179

DURADRY AM (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYCINE)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Duradry AM BarcaDuradry AM Barca

Duradry AM Clear SkyDuradry AM Clear Sky

Duradry AM End GameDuradry AM End Game

Duradry AM LimitlessDuradry AM Limitless

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69990-315-012026-01-29C16284748780-149896155-a28a-586f-e063-e6dba90add90DURADRY AM Deodorant & Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69990-315-01Duradry AM Deodorant and Antiperspirant65 g in 1 CYLINDERSTICK654
69990-315-01Duradry AM Deodorant and Antiperspirant1 in 1 CYLINDERSTICK14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69990-315DURADRY AM DEODORANT AND ANTIPERSPIRANT (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYCINE) STICK [NOVADORE USA INC]42 package rows20231111_b9e5c666-8f5f-afa2-e053-2a95a90a3940.zip

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
69990-31569990-315-01

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

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
09d2c6cd-1a36-8326-e063-6394a90a9803b9e5c666-8f5f-afa2-e053-2a95a90a39402023-11-10WarningsExact identifier
spl id: 09d2c6cd-1a36-8326-e063-6394a90a9803
spl set id: b9e5c666-8f5f-afa2-e053-2a95a90a3940

Reported adverse events (FAERS/openFDA)#

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