DURADRY ANTIPERSPIRANT BODY WIPES- aluminum chlohydrate cloth

Duradry Antiperspirant Body Wipes by

Drug Labeling and Warnings

Duradry Antiperspirant Body Wipes 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 Chlorohydrate 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 thoroughly before applying. Wipe body/hands/feet and let air dry. Wash off the next morning. Apply as needed during the day.

Inactive ingredients

Calcium Chloride, Caprylyl Glycol, Disodium EDTA, Ethylhexylglycerin, Glycine, Hydroxyacetophenone, Sodium Citrate, Water.

Questions?

Learn more at duradry.com

Dist. by Novadore USA LLC

Miami, FL 33179

Duradry Antiperspirant Body Wipes (Aluminum Chlorohydrate)

INGREDIENTS AND APPEARANCE

DURADRY ANTIPERSPIRANT BODY WIPES 
aluminum chlohydrate cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69990-401
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	200 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
GLYCINE (UNII: TE7660XO1C)
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69990-401-01	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)