Antiperspirant Deodorant Extra Dry Men

Manufacturer
Aruba Aloe Balm NV
Effective date
2023-11-06
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:59:15

Label at a glance#

ProductAntiperspirant Deodorant Extra Dry Men
Active ingredientALUMINUM CHLOROHYDRATE
Label structure6 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 Chlorohydrate 25%

Purpose

OTC - PURPOSE SECTION

antiperspirant

Uses:

INDICATIONS & USAGE SECTION

Reduces underarm perspiration

Warnings:

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

on broken skin.

Stop use an ask a doctor

OTC - STOP USE SECTION

if rash or irritation occurs.  Ask a doctor before use if you have kindney disease.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions:

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua/Eau), Glyceryl Stearate, Caprylic/Capric Triglyceride, Ceteareth-20, Cetereth-21, Cetyl Alcohol, Aloe Barbadensis Leaf Juice (Aloe Vera Gel from Aruba), Fragrance (Parfum), Phenoxyethanol, Caprylyl Glycol, Chlorphenesin, Propylene Glycol, Methylcellulose.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53675-161-00Antiperspirant Deodorant Extra Dry Men50 mL in 1 BOTTLELOTION504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53675-161ANTIPERSPIRANT DEODORANT EXTRA DRY MEN (ALUMINUM CHLOROHYDRATE) LOTION [ARUBA ALOE BALM NV]4Legacy NDC, 1 package rows20231108_30f98a0b-2bd3-4dae-b323-233ee207505f.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53675-16153675-161-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
54b07df0-2da6-b2b2-e063-6394a90a0f4830f98a0b-2bd3-4dae-b323-233ee207505f2026-06-20WarningsExact identifier
spl set id: 30f98a0b-2bd3-4dae-b323-233ee207505f

Reported adverse events (FAERS/openFDA)#

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