MITCHUM SENSITIVE SKIN- aluminum zirconium tetrachlorohydrex gly liquid liquid

Mitchum Sensitive Skin by

Drug Labeling and Warnings

Mitchum Sensitive Skin by is a Otc medication manufactured, distributed, or labeled by Revlon Consumer Products Corp, REVLON, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Aluminum Zirconium Tetrachlorohydrex Gly 20%

Purpose

Antiperspirant

WARNINGS

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 irriation occurs

Keep out of reach of children

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

INACTIVE INGREDIENT

Inactive Ingredients

Cyclopentasiloxane, Stearyl Alcohol, Isopropyl Myristate, Dimethicone, Hydrogenated Castor Oil, Talc, Petrolatum, PEG-23 Glyceryl Distearate, Aloe Barbadensis Leaf Extract, Allantoin, Tocopheryl Acetate

INDICATIONS & USAGE

Reduces underarm wetness

DOSAGE & ADMINISTRATION

Directions

Apply to underarms only

PRINCIPAL DISPLAY PANEL

Mitchum Sensitive

INGREDIENTS AND APPEARANCE

MITCHUM SENSITIVE SKIN 
aluminum zirconium tetrachlorohydrex gly liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-634
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY - UNII:8O386558JE)	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	0.2 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
DIMETHICONE (UNII: 92RU3N3Y1O)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
TALC (UNII: 7SEV7J4R1U)
PETROLATUM (UNII: 4T6H12BN9U)
PEG-23 GLYCERYL DISTEARATE (UNII: 527412VE0U)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALLANTOIN (UNII: 344S277G0Z)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-634-27	79 mL in 1 CONTAINER; Type 0: Not a Combination Product	10/05/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	10/05/2015

Labeler - Revlon Consumer Products Corp (788820165)

Establishment
Name	Address	ID/FEI	Business Operations
REVLON, INC.		809725570	manufacture(10967-634)