Label: DEGREE- advanced cool rush 72h antiperspirant deodorant stick

  • 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 March 17, 2023

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

  • Drug Facts

    Active ingredient

    Aluminum Sesquichlorohydrate (16%)

  • 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

    Cyclopentasiloxane, PPG-14 Butyl Ether, Stearyl Alcohol, Glycine, C12-15 Alkyl Benzoate, Hydrogenated Castor Oil, Fragrance (Parfum), Calcium Chloride, PEG-8 Distearate, Talc, Sodium Starch Octenylsuccinate, Silica, Maltodextrin, Hydrolyzed Corn Starch Octenylsuccinate, BHT.

  • Questions?

    Call toll-free 1-866-334-7331

  • Packaging

    Degree Men

  • INGREDIENTS AND APPEARANCE
    DEGREE 
    advanced cool rush 72h antiperspirant deodorant stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67751-223(NDC:64942-1933)
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V) ALUMINUM SESQUICHLOROHYDRATE16 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCINE (UNII: TE7660XO1C)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    PEG-8 DISTEARATE (UNII: 7JNC8VN07M)  
    TALC (UNII: 7SEV7J4R1U)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67751-223-011 in 1 BLISTER PACK07/19/2021
    114 g in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35007/19/2021
    Labeler - Navajo Manufacturing Company Inc. (091917799)
    Establishment
    NameAddressID/FEIBusiness Operations
    Navajo Manufacturing Company Inc.136941411relabel(67751-223) , repack(67751-223)