DURADRY PM- aluminum chloride hexahydrate gel

DURADRY PM by

Drug Labeling and Warnings

DURADRY PM by is a Otc medication manufactured, distributed, or labeled by Novadore USA, LLC. 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.
• Skin must be clean and completely dry.
• 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?

Visit us at www.duradry.com

Distributed by:
NOVADORE USA, INC
Miami, FL

DURADRY PM (ALUMINUM CHLORIDE HEXAHYDRATE)

INGREDIENTS AND APPEARANCE

DURADRY PM 
aluminum chloride hexahydrate gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69990-100
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)
SALICYLIC ACID (UNII: O414PZ4LPZ)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69990-100-01	1 in 1 CARTON	01/01/2015
1		50 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
2	NDC: 69990-100-02	1 in 1 CARTON	02/20/2018
2		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 final	part350	01/01/2015

Labeler - Novadore USA, LLC (079777451)

Registrant - Novadore USA, LLC (079777451)

Establishment
Name	Address	ID/FEI	Business Operations
Novadore USA, LLC		079777451	label(69990-100)