DOVE- advanced care invisible clear finish dry spray 72h antiperspirant deodorant aerosol, spray

Dove by

Drug Labeling and Warnings

Dove by is a Otc medication manufactured, distributed, or labeled by Conopco, Inc. d/b/a Unilever. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOVE ADVANCED CARE INVISIBLE CLEAR FINISH DRY SPRAY 72H ANTIPERSPIRANT DEODORANT - aluminum sesquichlorohydrate aerosol, spray

Drug Facts

Active ingredient

Aluminum Sesquichlorohydrate (12.2)

Purpose

antiperspirant

Uses

reduces underarm wetness

Warnings

FLAMMABLE. DO NOT USE NEAR HEAT, FLAME, OR WHILE SMOKING. CAN CAUSE SERIOUS INJURY OR DEATH
Keep away from face and mouth to avoid breathing in.
Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120°F/50°C or in enclosed places that could overheat
Do not use on broken skin. Stop use if rash or irritation occurs.
Ask a doctor before using if you have kidney disease.
USE ONLY AS DIRECTED. INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL.
Help stop inhalation abuse. For information visit www.inhalant.org

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Directions

apply to underarms only

Inactive ingredients

Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Isobutane, PPG-14 Butyl Ether, Glycine, Helianthus Annuus (Sunflower) Seed Oil, Fragrance (Parfum), C12-15 Alkyl Benzoate, Disteardimonium Hectorite, Calcium Chloride, Propane, BHT, Octyldodecanol, Propylene Carbonate, Dimethiconol, Benzyl Alcohol, Benzyl Benzoate, Citronellol, Geraniol, Hexyl Cinnamal, Limonene, Linalool

Questions?

Call toll-free 1-800-761-3683

Packaging

INGREDIENTS AND APPEARANCE

DOVE 
advanced care invisible clear finish dry spray 72h antiperspirant deodorant aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-2241
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V)	ALUMINUM SESQUICHLOROHYDRATE	12.2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
LIMONENE, (+)- (UNII: GFD7C86Q1W)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
BUTANE (UNII: 6LV4FOR43R)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
GLYCINE (UNII: TE7660XO1C)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
ISOBUTANE (UNII: BXR49TP611)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
SUNFLOWER OIL (UNII: 3W1JG795YI)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
PROPANE (UNII: T75W9911L6)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
OCTYLDODECANOL (UNII: 461N1O614Y)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
DIMETHICONOL (40 CST) (UNII: 343C7U75XW)
GERANIOL (UNII: L837108USY)
BENZYL BENZOATE (UNII: N863NB338G)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-2241-1	107 g in 1 CAN; Type 0: Not a Combination Product	12/01/2023
2	NDC: 64942-2241-2	136 g in 1 CAN; Type 0: Not a Combination Product	12/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	12/01/2023

Labeler - Conopco, Inc. d/b/a Unilever (001375088)