Label: CLINICAL STRENGTH MIRACLEDRY ANTIPERSPIRANT DEODORANT PM- aluminum chloride liquid

  • NDC Code(s): 53897-001-01
  • Packager: Highland Consumer Products
  • 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 January 5, 2022

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

  • Drug Facts


  • Active Ingredient

    Aluminum Chloride Hexahydrate 12%

  • PURPOSE

    Antiperspirant

  • Uses

    Treats excessive perspiration and reduces underarm wetness and odor.

  • Warnings

    For external use only

    Do not use

    on irritated skin.

    Keep out of reach of children

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

    Stop use and contact a doctor

    if rash or irritation develops

    Ask your doctor

    before using if you have kidney disease

  • Directions

    Apply to underarms only.  Use every other night or as needed (e.g. every night or every 3rd nights).  Apply only at bedtime.  Apply few strokes to underarms after tipping bottle to get maximum effect.

  • Inactive Ingredients

    Water, PPG-11 Stearyl Ether, Cyclopentasiloxane, Steareth-2, Glycine, Steareth-20, Zinc Oxide, Sodium Bicarbonate, Isopropyl Myristate,  Steareth-21

  • Storage

    Keep at room temperature

  • Questions?

    www.miracledry.com

  • PRINCIPAL DISPLAY PANEL

    clinical strength   Miracle Dry  ANTIPERSPIRANT DEODORANT   PM  NIGHT formula    1.2 FL OZ   35.5 ML

  • Product Label

    Miracle Dry PM

  • INGREDIENTS AND APPEARANCE
    CLINICAL STRENGTH MIRACLEDRY ANTIPERSPIRANT DEODORANT PM  
    aluminum chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53897-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE12 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PPG-11 STEARYL ETHER (UNII: S4G2J0Y0LG)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    STEARETH-2 (UNII: V56DFE46J5)  
    GLYCINE (UNII: TE7660XO1C)  
    STEARETH-20 (UNII: L0Q8IK9E08)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    STEARETH-21 (UNII: 53J3F32P58)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53897-001-0135.5 mL in 1 BOTTLE; Type 0: Not a Combination Product12/19/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35010/15/2012
    Labeler - Highland Consumer Products (078647762)
    Establishment
    NameAddressID/FEIBusiness Operations
    Englewood Lab, Inc.080987545manufacture(53897-001)