Duradry PM Sweat Minimizing Antiperspirant Gel

Manufacturer
Novadore USA Inc
Effective date
2023-11-10
Label type
HUMAN OTC DRUG LABEL
Version
12
Source
full-release
Hydrated at
2026-05-31 23:59:51

Label at a glance#

ProductDuradry PM Sweat Minimizing Antiperspirant Gel
Active ingredientALUMINUM CHLORIDE
Label structure11 sections

Indications and uses

Reduces underarm perspiration

Dosage and administration

Apply to underarms only. Apply a small amount of product to underarms at bedtime. It may itch during initial application. The next morning, rinse underarms with abundant water and apply a regular antiperspirant. For best results, use DURADRY® AM. Apply DURADRY® PM for a few nights in a row or until the excessive perspiration is controlled. Then Apply twice a week or as needed for maintenance.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

ALUMINUM CHLORIDE (HEXAHYDRATE) 15%

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, irritated or recently shaved skin.
  • Immediately after bathing.
  • In or near eyes. If contact occurs, rise eyes thoroughly with water.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply to underarms only.
  • Apply a small amount of product to underarms at bedtime. It may itch during initial application.
  • The next morning, rinse underarms with abundant water and apply a regular antiperspirant. For best results, use DURADRY® AM.
  • Apply DURADRY® PM for a few nights in a row or until the excessive perspiration is controlled. Then Apply twice a week or as needed for maintenance.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Propylene Glycol, Xanthan Gum, Sodium Bicarbonate,Disodium EDTA, Salicylic Acid.

Questions?

OTC - QUESTIONS SECTION

Learn more at duradry.com

Dist. by:

NOVADORE USA, LLC
Miami, FL 33179

DURADRY PM (ALUMINUM CHLORIDE HEXAHYDRATE)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

pm-tubepm-tube

pm-pouchpm-pouch

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69990-102-01Duradry PM Sweat Minimizing Antiperspirant Gel10.5 mL in 1 TUBEGEL10.512
69990-102-01Duradry PM Sweat Minimizing Antiperspirant Gel1 in 1 POUCHGEL112

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69990-102DURADRY PM SWEAT MINIMIZING ANTIPERSPIRANT GEL (ALUMINUM CHLORIDE HEXAHYDRATE) GEL [NOVADORE USA INC]122 package rows20231111_561bde06-d864-4d34-a330-d16cf5b6abff.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69990-10269990-102-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
09d141b4-b9b2-37ff-e063-6294a90ad5d2561bde06-d864-4d34-a330-d16cf5b6abff2023-11-10WarningsExact identifier
spl id: 09d141b4-b9b2-37ff-e063-6294a90ad5d2
spl set id: 561bde06-d864-4d34-a330-d16cf5b6abff

Reported adverse events (FAERS/openFDA)#

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