FDA.reportPublic FDA data

Duradry Antiperspirant Body Wipes

Manufacturer
Novadore USA Inc
Effective date
2024-10-20
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:27:39

Label at a glance#

ProductDuradry Antiperspirant Body Wipes
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Indications and uses

Reduces perspiration

Dosage and administration

Apply at bedtime. Wash and dry thoroughly before applying. Wipe body/hands/feet and let air dry. Wash off the next morning. Apply as needed during the day.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 20%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

Reduces perspiration

Warnings

WARNINGS SECTION

For external use only.

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.

Stop use

OTC - STOP USE SECTION

if rash or irritation occurs.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply at bedtime. Wash and dry thoroughly before applying. Wipe body/hands/feet and let air dry. Wash off the next morning. Apply as needed during the day.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Calcium Chloride, Caprylyl Glycol, Disodium EDTA, Ethylhexylglycerin, Glycine, Hydroxyacetophenone, Sodium Citrate, Water.

Questions?

OTC - QUESTIONS SECTION

Learn more at duradry.com

Dist. by Novadore USA LLC

Miami, FL 33179

Duradry Antiperspirant Body Wipes (Aluminum Chlorohydrate)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Duradry Antiperspirant Body WipesDuradry Antiperspirant Body Wipes

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69990-401-01Duradry Antiperspirant Body Wipes30 in 1 POUCHCLOTH305
69990-401-01Duradry Antiperspirant Body Wipes155 mL in 1 POUCHCLOTH1555

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69990-401DURADRY ANTIPERSPIRANT BODY WIPES (ALUMINUM CHLOHYDRATE) CLOTH [NOVADORE USA INC]52 package rows20241022_24eb6e93-fe52-d2f7-e063-6394a90a70f3.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69990-40169990-401-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
CALCIUM CHLORIDEM4I0D6VV5MIACT
GLYCINETE7660XO1CIACT
WATER059QF0KO0RIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
EDETATE DISODIUM7FLD91C86KIACT
SODIUM CITRATE1Q73Q2JULRIACT
CAPRYLYL GLYCOL00YIU5438UIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT

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
24ebf6e5-b28c-876e-e063-6394a90a00e024eb6e93-fe52-d2f7-e063-6394a90a70f32024-10-20WarningsExact identifier
spl id: 24ebf6e5-b28c-876e-e063-6394a90a00e0
spl set id: 24eb6e93-fe52-d2f7-e063-6394a90a70f3

Reported adverse events (FAERS/openFDA)#

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