Label: DEGREE- motionsense dry spray basil and lavender 48h antiperspirant deodorant aerosol, spray

  • NDC Code(s): 64942-1769-1
  • Packager: Conopco, Inc. d/b/a Unilever
  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated December 7, 2022

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  • DEGREE MOTIONSENSE DRY SPRAY BASIL & LAVENDER 48H ANTIPERSPIRANT DEODORANT - aluminum chlorohydrate aerosol, spray

    Degree Motionsense Dry Spray Basil & Lavender 48H Antiperspirant Deodorant

  • Drug Facts

    Active ingredient

    Aluminum Chlorohydrate (23.3%)

  • 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, Cyclopentasiloxane, I Hydrofluorocarbon 152a, Isobutane, PPG-14 Butyl Ether, Fragrance (Parfum), Disteardimonium Hectorite, Propane, BHT, Caprylic/Capric Triglyceride, Sodium Starch Octenylsuccinate, Propylene Carbonate, Maltodextrin, Hydrated Silica, Hydrolyzed Corn Starch Octenylsuccinate, Gelatin Crosspolymer, Silica, Cellulose Gum, Sodium Benzoate

  • Questions?

    Call toll-free 1-866-334-7331

  • Packaging

    DegreeDrySprayBasilLavenderAPDeoAE

  • INGREDIENTS AND APPEARANCE
    DEGREE 
    motionsense dry spray basil and lavender 48h antiperspirant deodorant aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1769
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE23.3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    BUTANE (UNII: 6LV4FOR43R)  
    1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    ISOBUTANE (UNII: BXR49TP611)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    PROPANE (UNII: T75W9911L6)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1769-1107 g in 1 CAN; Type 0: Not a Combination Product10/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35010/15/2020
    Labeler - Conopco, Inc. d/b/a Unilever (001375088)