REVLON MITCHUM CLINICAL STRENGTH SOFT SOLID- aluminum zirconium tetrachlorohydrex gly liquid REVLON MITCHUM CLINICAL STRENGTH SOFT SOLID- aluminum zirconium tetrachlorohydrex gly liquid liquid

Revlon Mitchum Clinical Strength Soft Solid by

Drug Labeling and Warnings

Revlon Mitchum Clinical Strength Soft Solid by is a Otc medication manufactured, distributed, or labeled by Revlon Consumer Products Corp, DMI. 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, TRIBEHENIN, DIMETHICONE, PETROLATUM, TRISILOXANE, C18-36 ACID TRIGLYCERIDE, AQUA ((WATER) EAU), PARFUM (FRAGRANCE), SODIUM STARCH OCTENYLSUCCINATE, SILICA DIMETHICONE SILYLATE, ISOPROPYL MYRISTATE, ETHYLENE BRASSYLATE, BENZYL ALCOHOL, HYDROGEN PEROXIDE, TOCOPHERYL ACETATE, ALOE BARBADENSIS LEAF EXTRACT, HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE, HYDROXYCITRONELLAL, CITRONELLOL, ALPHA-ISOMETHYL IONONE, MANNITOL, SILICA, GERANIOL, BHT, SODIUM ASCORBATE, CITRIC ACID, CALCIUM DISODIUM EDTA

INDICATIONS & USAGE

Reduces underarm wetness

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

Revlon Mitchum Clinical Strength Soft Solid

PRINCIPAL DISPLAY PANEL

Revlon Mitchum Clinical Strength Soft Solid

PRINCIPAL DISPLAY PANEL

Revlon Mitchum Clinical Strength Soft Solid

PRINCIPAL DISPLAY PANEL

Revlon Mitchum Clinical Strength Soft Solid

PRINCIPAL DISPLAY PANEL

Revlon Mitchum Clinical Strength Soft Solid

PRINCIPAL DISPLAY PANEL

Revlon Mitchum Clinical Strength Soft Solid

INGREDIENTS AND APPEARANCE

REVLON MITCHUM CLINICAL STRENGTH SOFT SOLID 
aluminum zirconium tetrachlorohydrex gly liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-624
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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MANNITOL (UNII: 3OWL53L36A)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
GERANIOL (UNII: L837108USY)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SODIUM ASCORBATE (UNII: S033EH8359)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DIMETHICONE (UNII: 92RU3N3Y1O)
PETROLATUM (UNII: 4T6H12BN9U)
TRISILOXANE (UNII: 9G1ZW13R0G)
C18-36 ACID TRIGLYCERIDE (UNII: ZRA72DR3R7)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
BENZYL ALCOHOL (UNII: LKG8494WBH)
HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-624-24	70 mL in 1 CONTAINER; Type 0: Not a Combination Product	01/01/2014
2	NDC: 10967-624-16	47 mL in 1 CONTAINER; Type 0: Not a Combination Product	01/01/2014
3	NDC: 10967-624-50	14 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

REVLON MITCHUM CLINICAL STRENGTH SOFT SOLID 
aluminum zirconium tetrachlorohydrex gly liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-626
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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MANNITOL (UNII: 3OWL53L36A)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
GERANIOL (UNII: L837108USY)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SODIUM ASCORBATE (UNII: S033EH8359)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DIMETHICONE (UNII: 92RU3N3Y1O)
PETROLATUM (UNII: 4T6H12BN9U)
TRISILOXANE (UNII: 9G1ZW13R0G)
C18-36 ACID TRIGLYCERIDE (UNII: ZRA72DR3R7)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
BENZYL ALCOHOL (UNII: LKG8494WBH)
HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-626-24	70 mL in 1 CONTAINER; Type 0: Not a Combination Product	01/01/2014
2	NDC: 10967-626-16	47 mL in 1 CONTAINER; Type 0: Not a Combination Product	01/01/2014
3	NDC: 10967-626-50	14 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

REVLON MITCHUM CLINICAL STRENGTH SOFT SOLID 
aluminum zirconium tetrachlorohydrex gly liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-627
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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MANNITOL (UNII: 3OWL53L36A)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
GERANIOL (UNII: L837108USY)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SODIUM ASCORBATE (UNII: S033EH8359)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DIMETHICONE (UNII: 92RU3N3Y1O)
PETROLATUM (UNII: 4T6H12BN9U)
TRISILOXANE (UNII: 9G1ZW13R0G)
C18-36 ACID TRIGLYCERIDE (UNII: ZRA72DR3R7)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
BENZYL ALCOHOL (UNII: LKG8494WBH)
HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-627-24	70 mL in 1 CONTAINER; Type 0: Not a Combination Product	01/01/2014
2	NDC: 10967-627-16	47 mL in 1 CONTAINER; Type 0: Not a Combination Product	01/01/2014
3	NDC: 10967-627-50	14 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

REVLON MITCHUM CLINICAL STRENGTH SOFT SOLID 
aluminum zirconium tetrachlorohydrex gly liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-646
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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MANNITOL (UNII: 3OWL53L36A)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
GERANIOL (UNII: L837108USY)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SODIUM ASCORBATE (UNII: S033EH8359)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DIMETHICONE (UNII: 92RU3N3Y1O)
PETROLATUM (UNII: 4T6H12BN9U)
TRISILOXANE (UNII: 9G1ZW13R0G)
C18-36 ACID TRIGLYCERIDE (UNII: ZRA72DR3R7)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
BENZYL ALCOHOL (UNII: LKG8494WBH)
HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-646-24	70 mL in 1 CONTAINER; Type 0: Not a Combination Product	01/01/2014
2	NDC: 10967-646-16	47 mL in 1 CONTAINER; Type 0: Not a Combination Product	01/01/2014
3	NDC: 10967-646-50	14 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

REVLON MITCHUM CLINICAL STRENGTH SOFT SOLID 
aluminum zirconium tetrachlorohydrex gly liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-625
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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MANNITOL (UNII: 3OWL53L36A)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
GERANIOL (UNII: L837108USY)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SODIUM ASCORBATE (UNII: S033EH8359)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DIMETHICONE (UNII: 92RU3N3Y1O)
PETROLATUM (UNII: 4T6H12BN9U)
TRISILOXANE (UNII: 9G1ZW13R0G)
C18-36 ACID TRIGLYCERIDE (UNII: ZRA72DR3R7)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
BENZYL ALCOHOL (UNII: LKG8494WBH)
HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-625-16	47 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

REVLON MITCHUM CLINICAL STRENGTH SOFT SOLID 
aluminum zirconium tetrachlorohydrex gly liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-641
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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MANNITOL (UNII: 3OWL53L36A)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
GERANIOL (UNII: L837108USY)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SODIUM ASCORBATE (UNII: S033EH8359)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DIMETHICONE (UNII: 92RU3N3Y1O)
PETROLATUM (UNII: 4T6H12BN9U)
TRISILOXANE (UNII: 9G1ZW13R0G)
C18-36 ACID TRIGLYCERIDE (UNII: ZRA72DR3R7)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
BENZYL ALCOHOL (UNII: LKG8494WBH)
HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-641-16	47 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
DMI		076693183	manufacture(10967-624, 10967-626, 10967-627, 10967-646, 10967-625, 10967-641)