FDA.reportPublic FDA data

Sport Deodorant Extra Antiperspirant

Manufacturer
Aruba Aloe Balm NV
Effective date
2023-11-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:59:19

Label at a glance#

ProductSport Deodorant Extra Antiperspirant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure6 sections

Indications and uses

Reduces underarm perspiration

Dosage and administration

Shake well before use. 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 and ask a doctor

OTC - STOP USE SECTION

if rash or irritation occurs.

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

Directions:

DOSAGE & ADMINISTRATION SECTION

Shake well before use. Apply to underarms only.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua/Eau), Cetearyl Glucoside, Glyceryl Stearate, Caprylic/Capric Triglyceride, Sodium Stearoyl Glutamate, Ceteareth-20, Ceteareth-21, Cetearyl Alcohol, Aloe Barbadensis Leaf Juice (Aloe Vera Gel from Aruba), Fragrance (Parfum), Phenoxyethanol, Caprylyl Glycol, Chlorphenesin, Propylene Glycol, Sodium Hydroxide, Tocopheryl (Vitamin E) Acetate, Methylcellulose.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53675-204-00Sport Deodorant Extra Antiperspirant89 mL in 1 BOTTLELOTION892

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53675-204SPORT DEODORANT EXTRA ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) LOTION [ARUBA ALOE BALM NV]2Legacy NDC, 1 package rows20231108_6ff11d8a-61b1-422d-a5aa-a8f7a56a5331.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
53675-20453675-204-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CETEARYL GLUCOSIDE09FUA47KNAIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
SODIUM STEAROYL GLUTAMATE65A9F4P024IACT
POLYOXYL 20 CETOSTEARYL ETHERYRC528SWUYIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
ALOE VERA LEAFZY81Z83H0XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CAPRYLYL GLYCOL00YIU5438UIACT
CHLORPHENESINI670DAL4SZIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM HYDROXIDE55X04QC32IIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
METHYLCELLULOSE, UNSPECIFIEDZ944H5SN0HIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB

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
54b1fcb2-a1d3-ff18-e063-6394a90aa1126ff11d8a-61b1-422d-a5aa-a8f7a56a53312026-06-20WarningsExact identifier
spl set id: 6ff11d8a-61b1-422d-a5aa-a8f7a56a5331

Reported adverse events (FAERS/openFDA)#

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