DURADRY SWEAT MINIMIZING GEL- aluminum chloride hexahydrate gel

Duradry Sweat Minimizing Gel by

Drug Labeling and Warnings

Duradry Sweat Minimizing Gel by is a Otc medication manufactured, distributed, or labeled by Novadore USA Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

ALUMINUM CHLORIDE (HEXAHYDRATE) 15%

Purpose

Antiperspirant

Uses

Reduces underarm perspiration

Warnings

For external use only
Stop use if rash or irritation occurs.

Do not use

• On broken, irritated or recently shaved skin.
• Immediately after bathing.
• In or near eyes. If contact occurs, rise eyes thoroughly with water.

Ask a doctor before use

if you have kidney disease

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Apply to underarms only.
• Apply a small amount of product to underarms at bedtime. It may itch during initial application.
• The next morning, rinse underarms with abundant water and apply a regular antiperspirant. For best results, use DURADRY® AM.
• Apply DURADRY® PM for a few nights in a row or until the excessive perspiration is controlled. Then Apply twice a week or as needed for maintenance.

Inactive ingredients

Aqua, Propylene Glycol, Xanthan Gum, Sodium Bicarbonate,Disodium EDTA, Salicylic Acid.

Questions?

Learn more at duradry.com

Duradry Sweat Minimizing Gel (ALUMINUM CHLORIDE HEXAHYDRATE)

INGREDIENTS AND APPEARANCE

DURADRY SWEAT MINIMIZING GEL 
aluminum chloride hexahydrate gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69990-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B)	ALUMINUM CHLORIDE	150 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM (UNII: 7FLD91C86K)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)
SALICYLIC ACID (UNII: O414PZ4LPZ)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69990-103-01	1 in 1 POUCH	02/20/2018
1		10.5 mL 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 Drug	M019	01/01/2015

Labeler - Novadore USA Inc (079777451)

Registrant - Novadore USA Inc (079777451)