FDA.reportPublic FDA data

Aquax Deo

Manufacturer
Pella Pharmaceuticals Co. Ltd
Effective date
2021-11-25
Label type
HUMAN OTC DRUG LABEL
Version
313
Source
full-release
Hydrated at
2026-05-31 23:45:11

Label at a glance#

ProductAquax Deo
Active ingredientALUMINUM CHLOROHYDRATE
Label structure14 sections

Dosage and administration

Dry the area to be treated, and then apply Aquax ® Deo cream at night, at bed time

Storage and handling

Store at a temperature belwo 30 °C

Label contents#

Full prescribing information#

Forms and presentation

HOW SUPPLIED SECTION

Cream: Tube of 75 g

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua, Cetearyl Alcohol, Ceteareth-22, Glycerin, Petrolatum, Ceteareth-25, Sodium Citrate, Methylparaben, Citric Acid, Parfum, Propylparaben.

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Properties

DESCRIPTION SECTION

Aquax ® Deo cream reduces excessive sweating (hyperhidrosis)

Indications

INDICATIONS & USAGE SECTION

Aquax ® Deo cream is used to reduce excessive perspiraton (hyperhidrosis)

Precautions

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

Warnings

WARNINGS SECTION

  • For external use only
  • Do not apply to broken or irritated skin
  • Do not shave auxiliaries for 24 hours before application

Contraindications

CONTRAINDICATIONS SECTION

Hypersensitivity to any of the components

Side effects

ADVERSE REACTIONS SECTION

Aquax ® Deo cream has no known side effect, its us is without risk

Dosage and administration

DOSAGE & ADMINISTRATION SECTION

Dry the area to be treated, and then apply Aquax ® Deo cream at night, at bed time

Storage conditions

STORAGE AND HANDLING SECTION

Store at a temperature belwo 30 °C

Primary Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Primary PackagePrimary Package

Secondary Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Secondary PackageSecondary Package

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82160-313-01Aquax Deo1 in 1 CARTONCREAM1313
82160-313-01Aquax Deo75 g in 1 TUBECREAM75313

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82160-313AQUAX DEO (ALUMINUM CHLOROHYDRATE) CREAM [PELLA PHARMACEUTICALS CO. LTD]313Legacy NDC, 2 package rows20211130_d19b9a37-a05a-3de4-e053-2a95a90a50a8.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
82160-31382160-313-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
WATER059QF0KO0RIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
CETEARETH-2228VZG1E234IACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
PETROLATUM4T6H12BN9UIACT
CETEARETH-258FA93U5T67IACT
SODIUM CITRATE1Q73Q2JULRIACT
METHYLPARABENA2I8C7HI9TIACT
PROPYLPARABENZ8IX2SC1OHIACT
GLYCERINPDC6A3C0OXIACT

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
d19b9a37-a05b-3de4-e053-2a95a90a50a8d19b9a37-a05a-3de4-e053-2a95a90a50a82021-11-25Warnings, Adverse reactionsExact identifier
spl id: d19b9a37-a05b-3de4-e053-2a95a90a50a8
spl set id: d19b9a37-a05a-3de4-e053-2a95a90a50a8

Reported adverse events (FAERS/openFDA)#

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