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Clinical Strength MiracleDry Antiperspirant Deodorant PM

Medically reviewed on December 22, 2017

Dosage form: liquid
Ingredients: ALUMINUM CHLORIDE 12mg in 1mL
Labeler: Highland Consumer Products
NDC Code: 53897-001

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.

Clinical Strength MiracleDry Antiperspirant Deodorant PM

Drug Facts


Active Ingredient

Aluminum Chloride Hexahydrate 12%

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

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

Product Label

CLINICAL STRENGTH MIRACLEDRY ANTIPERSPIRANT DEODORANT PM  
aluminum chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53897-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLORIDE (ALUMINUM CATION) ALUMINUM CHLORIDE12 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
PPG-11 STEARYL ETHER 
CYCLOMETHICONE 5 
STEARETH-2 
GLYCINE 
STEARETH-20 
ZINC OXIDE 
SODIUM BICARBONATE 
ISOPROPYL MYRISTATE 
STEARETH-21 
Packaging
#Item CodePackage Description
1NDC:53897-001-0135.5 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35010/15/2012
Labeler - Highland Consumer Products (078647762)
Establishment
NameAddressID/FEIOperations
Englewood Lab, Inc.080366903manufacture(53897-001)
Establishment
NameAddressID/FEIOperations
Englewood Lab Inc690104005manufacture(53897-001)

 
Highland Consumer Products

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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