CLINICAL STRENGTH MIRACLEDRY ANTIPERSPIRANT DEODORANT PM- aluminum chloride liquid

Clinical Strength MiracleDry Antiperspirant Deodorant PM by

Drug Labeling and Warnings

Clinical Strength MiracleDry Antiperspirant Deodorant PM by is a Otc medication manufactured, distributed, or labeled by Highland Consumer Products, Englewood Lab, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

CLINICAL STRENGTH MIRACLEDRY ANTIPERSPIRANT DEODORANT PM  
aluminum chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53897-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B)	ALUMINUM CHLORIDE	12 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53897-001-01	35.5 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/19/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	10/15/2012

Labeler - Highland Consumer Products (078647762)

Establishment
Name	Address	ID/FEI	Business Operations
Englewood Lab, Inc.		080366903	manufacture(53897-001)

Establishment
Name	Address	ID/FEI	Business Operations
Englewood Lab Korea Co., Ltd.		690104005	manufacture(53897-001)