Label: DOVE- advanced coconut water and lime dry spray 72h antiperspirant deodorant aerosol, spray
- NDC Code(s): 64942-2131-1
- Packager: Conopco, Inc. d/b/a Unilever
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2024
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- Official Label (Printer Friendly)
- DOVE ADVANCED COCONUT WATER & LIME DRY SPRAY 72H ANTIPERSPIRANT DEODORANT - aluminum sesquichlorohydrate aerosol, spray
- Drug Facts
- Purpose
- Uses
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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
- Directions
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Inactive ingredients
Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Isobutane, PPG-14 Butyl Ether, Glycine, Fragrance (Parfum), Helianthus Annuus (Sunflower) Seed Oil, C12-15 Alkyl Benzoate, Disteardimonium Hectorite, Calcium Chloride, Propane, BHT, Octyldodecanol, Propylene Carbonate, Dimethiconol, Benzyl Alcohol, Citral, Citronellol, Geraniol, Hexyl Cinnamal, Limonene, Linalool.
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INGREDIENTS AND APPEARANCE
DOVE
advanced coconut water and lime dry spray 72h antiperspirant deodorant aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-2131 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V) ALUMINUM SESQUICHLOROHYDRATE 15.2 g in 100 g Inactive Ingredients Ingredient Name Strength GERANIOL (UNII: L837108USY) BENZYL ALCOHOL (UNII: LKG8494WBH) CALCIUM CHLORIDE (UNII: M4I0D6VV5M) LINALOOL, (+/-)- (UNII: D81QY6I88E) 1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) LIMONENE, (+)- (UNII: GFD7C86Q1W) GLYCINE (UNII: TE7660XO1C) BUTANE (UNII: 6LV4FOR43R) 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) CITRAL (UNII: T7EU0O9VPP) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-2131-1 107 g in 1 CAN; Type 0: Not a Combination Product 09/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M019 09/01/2023 Labeler - Conopco, Inc. d/b/a Unilever (001375088)
