Antiperspirant Deodorant Powder Fresh Women

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 23:59:28

Label at a glance#

ProductAntiperspirant Deodorant Powder Fresh Women

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 16%

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

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, Sodium Hydroxide, Tocopheryl (Vitamin E) Acetate.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label03

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
53675-202-01	Antiperspirant Deodorant Powder Fresh Women	89 mL in 1 BOTTLE	LOTION	89		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53675-202	ANTIPERSPIRANT DEODORANT POWDER FRESH WOMEN (ALUMINUM CHLOROHYDRATE) LOTION [ARUBA ALOE BALM NV]	2	Legacy NDC, 1 package rows	20231108_dd34cc33-f5cb-4e1c-abff-080019078e42.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

Antiperspirant Deodorant Powder Fresh Women
ALUMINUM CHLOROHYDRATE
WATER
CETEARYL GLUCOSIDE
GLYCERYL MONOSTEARATE
MEDIUM-CHAIN TRIGLYCERIDES
SODIUM STEAROYL GLUTAMATE
POLYOXYL 20 CETOSTEARYL ETHER
CETOSTEARYL ALCOHOL
ALOE VERA LEAF
PHENOXYETHANOL
CAPRYLYL GLYCOL
CHLORPHENESIN
SODIUM HYDROXIDE
.ALPHA.-TOCOPHEROL ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
53675-202	53675-202-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
CETEARYL GLUCOSIDE	09FUA47KNA	IACT
GLYCERYL MONOSTEARATE	230OU9XXE4	IACT
MEDIUM-CHAIN TRIGLYCERIDES	C9H2L21V7U	IACT
SODIUM STEAROYL GLUTAMATE	65A9F4P024	IACT
POLYOXYL 20 CETOSTEARYL ETHER	YRC528SWUY	IACT
CETOSTEARYL ALCOHOL	2DMT128M1S	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
CAPRYLYL GLYCOL	00YIU5438U	IACT
CHLORPHENESIN	I670DAL4SZ	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
ALUMINUM CHLOROHYDRATE	HPN8MZW13M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
54b1e9c3-c44e-93fb-e063-6294a90ae7f8			dd34cc33-f5cb-4e1c-abff-080019078e42	2026-06-20	Warnings	Exact identifier spl set id: dd34cc33-f5cb-4e1c-abff-080019078e42

Reported adverse events (FAERS/openFDA)#

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