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Clinical Strength MiracleDry Antiperspirant Deodorant PM

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

Medically reviewed on Dec 22, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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