MITCHUM ROLL ON- aluminum zirconium tetrachlorohydrex gly liquid

Mitchum Roll On by

Drug Labeling and Warnings

Mitchum Roll On 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

AQUA ((WATER) EAU), GLYCERYL STEARATE, LAURETH-23, MAGNESIUM ALUMINUM SILICATE, POLYSORBATE 20, PARFUM (FRAGRANCE), LAURETH-4, LAURIC ACID, CETEARYL ALCOHOL, EDTA, BENHENTRIMONIUM METHOSULFATE, BENZYL SALICYLATE, LINALOOL, SILICA DIMETHICONE SILYLATE, LIMONENE, HEXYL CINNAMAL, TOCOPHERYL ACETATE, ALOE BARBADENSIS LEAF EXTRACT, COUMARIN, HYDROGEN PEROXIDE, CITRONELLOL, GERANIOL

INDICATIONS & USAGE

Reduces underarm wetness

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

Mitchum Roll On

PRINCIPAL DISPLAY PANEL

Mitchum Roll On

INGREDIENTS AND APPEARANCE

MITCHUM ROLL ON 
aluminum zirconium tetrachlorohydrex gly liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-601
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
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
LAURETH-23 (UNII: N72LMW566G)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
LAURETH-4 (UNII: 6HQ855798J)
LAURIC ACID (UNII: 1160N9NU9U)
EDETIC ACID (UNII: 9G34HU7RV0)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
GERANIOL (UNII: L837108USY)
COUMARIN (UNII: A4VZ22K1WT)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
LIMONENE, (+/-)- (UNII: 9MC3I34447)
LINALOOL, (+/-)- (UNII: D81QY6I88E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-601-34	100 mL in 1 CONTAINER; Type 0: Not a Combination Product	01/01/2014
2	NDC: 10967-601-17	50 mL in 1 CONTAINER; Type 0: Not a Combination Product	01/01/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	01/01/2014

MITCHUM ROLL ON 
aluminum zirconium tetrachlorohydrex gly liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-609
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
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
LAURETH-23 (UNII: N72LMW566G)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
LAURETH-4 (UNII: 6HQ855798J)
LAURIC ACID (UNII: 1160N9NU9U)
EDETIC ACID (UNII: 9G34HU7RV0)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
GERANIOL (UNII: L837108USY)
COUMARIN (UNII: A4VZ22K1WT)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
LIMONENE, (+/-)- (UNII: 9MC3I34447)
LINALOOL, (+/-)- (UNII: D81QY6I88E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-609-17	50 mL in 1 CONTAINER; Type 0: Not a Combination Product	01/01/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	01/01/2014

Labeler - Revlon Consumer Products Corp (788820165)

Establishment
Name	Address	ID/FEI	Business Operations
REVLON, INC.		809725570	manufacture(10967-601, 10967-609)