AQUAX DEO- aluminum chlorohydrate cream

Aquax Deo by

Drug Labeling and Warnings

Aquax Deo by is a Otc medication manufactured, distributed, or labeled by Pella Pharmaceuticals Co. Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Forms and presentation

Cream: Tube of 75 g

Active Ingredient

Aluminum Chlorohydrate

Inactive Ingredients

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

Purpose

Antiperspirant

Properties

Aquax ® Deo cream reduces excessive sweating (hyperhidrosis)

Indications

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

Precautions

keep out of reach of children

Warnings

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

Contraindications

Hypersensitivity to any of the components

Side effects

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

Dosage and administration

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

Storage conditions

Store at a temperature belwo 30 °C

Primary Package

Secondary Package

INGREDIENTS AND APPEARANCE

AQUAX DEO 
aluminum chlorohydrate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82160-313
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	150 mg  in 75 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
CETEARETH-22 (UNII: 28VZG1E234)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
PETROLATUM (UNII: 4T6H12BN9U)
CETEARETH-25 (UNII: 8FA93U5T67)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82160-313-01	1 in 1 CARTON	03/15/2011
1		75 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	03/15/2011

Labeler - Pella Pharmaceuticals Co. Ltd (562370925)