DURADRY HANDS AND FEET ANTIPERSPIRANT WIPES- aluminum sesquichlorohydrate cloth

Duradry Hands and Feet Antiperspirant Wipes by

Drug Labeling and Warnings

Duradry Hands and Feet Antiperspirant Wipes 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 Sesquichlorohydrate 20%

Purpose

Antiperspirant

Uses

Reduces perspiration

Warnings

For external use only.

Do not use

on broken skin

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 immediately.

Stop use

if rash or irritation occurs.

Directions

Apply at bedtime. Wash and dry hands/feet thoroughly. Wipe hands/feet and let air dry. Wash off the next morning. Apply as needed during the day.

Inactive ingredients

Water, Caprylyl Glycol, Ethylhexylglycerin, Hydroxyacetophenone, Disodium EDTA, Sodium Citrate.

Questions?

Learn more at duradry.com

Dist. by Novadore USA LLC

Miami, FL 33179

Duradry Antiperspirant Wipes (aluminum sesquichlorohydrate)

INGREDIENTS AND APPEARANCE

DURADRY HANDS AND FEET ANTIPERSPIRANT WIPES 
aluminum sesquichlorohydrate cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69990-400
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V)	ALUMINUM SESQUICHLOROHYDRATE	200 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
WATER (UNII: 059QF0KO0R)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69990-400-01	30 in 1 POUCH	03/29/2022
1		155 mL in 1 POUCH; 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	03/29/2022

Labeler - Novadore USA Inc (079777451)

Registrant - Novadore USA Inc (079777451)