Label: DOVE- coconut and hibiscus fresh 48h antiperspirant deodorant stick

  • NDC Code(s): 64942-2148-1
  • Packager: Conopco Inc. d/b/a/ Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated August 22, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • SHEA MOISTURE COCONUT & HIBISCUS FRESH 48H ANTIPERSPIRANT DEODORANT - aluminum sesquichlorohydrate stick

  • Drug Facts

    Active ingredient

    Aluminum Sesquichlorohydrate (12.2)

  • Purpose

    antiperspirant

  • Uses

    reduces underarm wetness

  • Warnings

    • For external use only.
    • Do not use on broken skin .
    • Ask a doctor before use if you have     kidney disease.
    • Stop use if rash or irritation occurs.

  • KEEP OUT OF REACH OF CHILDREN

    • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    apply to underarms only

  • Inactive ingredients

    Water (Aqua), C12-15 Alkyl Benzoate, Cyclopentasiloxane, Synthetic Wax, Glycerin, Calcium Chloride, Cetyl PEG/PPG-10/1 Dimethicone, Glycine, Fragrance (Parfum), Helianthus Annuus (Sunflower) Seed Oil, Butyrospermum Parkii (Shea) Butter, Cocos Nucifera (Coconut) Oil, Hibiscus Rosa Sinensis Flower Extract, Benzyl Alcohol, Benzyl Benzoate, Benzyl Salicylate, Citral, Coumarin, Hydroxycitronellal, Limonene.

  • Questions?

    Call 1-800-761-3683

  • Packaging

    Shea Moisture Fresh AP Deo

  • INGREDIENTS AND APPEARANCE
    DOVE 
    coconut and hibiscus fresh 48h antiperspirant deodorant stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-2148
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V) ALUMINUM SESQUICHLOROHYDRATE12.2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CITRAL (UNII: T7EU0O9VPP)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    BENZYL BENZOATE (UNII: N863NB338G)  
    HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    WATER (UNII: 059QF0KO0R)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETYL PEG/PPG-10/1 DIMETHICONE (HLB 4) (UNII: 8INO2K35FA)  
    GLYCINE (UNII: TE7660XO1C)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    HIBISCUS ROSA-SINENSIS FLOWER (UNII: VB092Y7Z8T)  
    COUMARIN (UNII: A4VZ22K1WT)  
    BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-2148-174 g in 1 CONTAINER; Type 0: Not a Combination Product10/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35010/01/2023
    Labeler - Conopco Inc. d/b/a/ Unilever (001375088)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!