Label: MITCHUM ADVANCED CONTROL SOLID- aluminum zirconium tetrachlorohydrex gly liquid liquid
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NDC Code(s):
10967-617-27,
10967-618-27,
10967-619-27,
10967-620-27, view more10967-629-27, 10967-644-27, 10967-645-27
- Packager: Revlon Consumer Products Corp
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 30, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Purpose
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
Inactive Ingredients
CYCLOPENTASILOXANE, STEARYL ALCOHOL, PPG-14 BUTYL ETHER, TALC, PARFUM (FRAGRANCE), HYDROGENATED CASTOR OIL, PEG-8 DISTEARATE, SODIUM STARCH OCTENYLSUCCINATE, TOCOPHERYL ACETATE, ALOE BARBADENSIS LEAF EXTRACT, MANNITOL, AQUA ((WATER) EAU), CITRONELLOL, GERANIOL, SILICA DIMETHICONE SILYLATE, SILICA, COUMARIN, HYDROGEN PEROXIDE, LIMONENE, LINALOOL, ISOEUGENOL, CALCIUM DISODIUM EDTA, BHT, SODIUM ASCORBATE, CITRIC ACID, CITRAL
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MITCHUM ADVANCED CONTROL SOLID
aluminum zirconium tetrachlorohydrex gly liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10967-629 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) PPG-14 BUTYL ETHER (UNII: R199TJT95T) TALC (UNII: 7SEV7J4R1U) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) PEG-8 DISTEARATE (UNII: 7JNC8VN07M) .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) COUMARIN (UNII: A4VZ22K1WT) HYDROGEN PEROXIDE (UNII: BBX060AN9V) LIMONENE, (+/-)- (UNII: 9MC3I34447) LINALOOL, (+/-)- (UNII: D81QY6I88E) ISOEUGENOL (UNII: 5M0MWY797U) EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) SODIUM ASCORBATE (UNII: S033EH8359) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CITRAL (UNII: T7EU0O9VPP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10967-629-27 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 Drug M019 01/01/2014 12/31/2024 MITCHUM ADVANCED CONTROL SOLID
aluminum zirconium tetrachlorohydrex gly liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10967-617 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) PPG-14 BUTYL ETHER (UNII: R199TJT95T) TALC (UNII: 7SEV7J4R1U) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) PEG-8 DISTEARATE (UNII: 7JNC8VN07M) .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) COUMARIN (UNII: A4VZ22K1WT) HYDROGEN PEROXIDE (UNII: BBX060AN9V) LIMONENE, (+/-)- (UNII: 9MC3I34447) LINALOOL, (+/-)- (UNII: D81QY6I88E) ISOEUGENOL (UNII: 5M0MWY797U) EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) SODIUM ASCORBATE (UNII: S033EH8359) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CITRAL (UNII: T7EU0O9VPP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10967-617-27 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 Drug M019 01/01/2014 12/31/2024 MITCHUM ADVANCED CONTROL SOLID
aluminum zirconium tetrachlorohydrex gly liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10967-618 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) PPG-14 BUTYL ETHER (UNII: R199TJT95T) TALC (UNII: 7SEV7J4R1U) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) PEG-8 DISTEARATE (UNII: 7JNC8VN07M) .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) COUMARIN (UNII: A4VZ22K1WT) HYDROGEN PEROXIDE (UNII: BBX060AN9V) LIMONENE, (+/-)- (UNII: 9MC3I34447) LINALOOL, (+/-)- (UNII: D81QY6I88E) ISOEUGENOL (UNII: 5M0MWY797U) EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) SODIUM ASCORBATE (UNII: S033EH8359) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CITRAL (UNII: T7EU0O9VPP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10967-618-27 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 Drug M019 01/01/2014 12/31/2024 MITCHUM ADVANCED CONTROL SOLID
aluminum zirconium tetrachlorohydrex gly liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10967-644 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) PPG-14 BUTYL ETHER (UNII: R199TJT95T) TALC (UNII: 7SEV7J4R1U) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) PEG-8 DISTEARATE (UNII: 7JNC8VN07M) .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) COUMARIN (UNII: A4VZ22K1WT) HYDROGEN PEROXIDE (UNII: BBX060AN9V) LIMONENE, (+/-)- (UNII: 9MC3I34447) LINALOOL, (+/-)- (UNII: D81QY6I88E) ISOEUGENOL (UNII: 5M0MWY797U) EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) SODIUM ASCORBATE (UNII: S033EH8359) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CITRAL (UNII: T7EU0O9VPP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10967-644-27 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 Drug M019 01/01/2014 MITCHUM ADVANCED CONTROL SOLID
aluminum zirconium tetrachlorohydrex gly liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10967-619 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) PPG-14 BUTYL ETHER (UNII: R199TJT95T) TALC (UNII: 7SEV7J4R1U) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) PEG-8 DISTEARATE (UNII: 7JNC8VN07M) .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) COUMARIN (UNII: A4VZ22K1WT) HYDROGEN PEROXIDE (UNII: BBX060AN9V) LIMONENE, (+/-)- (UNII: 9MC3I34447) LINALOOL, (+/-)- (UNII: D81QY6I88E) ISOEUGENOL (UNII: 5M0MWY797U) EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) SODIUM ASCORBATE (UNII: S033EH8359) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CITRAL (UNII: T7EU0O9VPP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10967-619-27 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 Drug M019 01/01/2014 12/31/2024 MITCHUM ADVANCED CONTROL SOLID
aluminum zirconium tetrachlorohydrex gly liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10967-620 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) PPG-14 BUTYL ETHER (UNII: R199TJT95T) TALC (UNII: 7SEV7J4R1U) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) PEG-8 DISTEARATE (UNII: 7JNC8VN07M) .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) COUMARIN (UNII: A4VZ22K1WT) HYDROGEN PEROXIDE (UNII: BBX060AN9V) LIMONENE, (+/-)- (UNII: 9MC3I34447) LINALOOL, (+/-)- (UNII: D81QY6I88E) ISOEUGENOL (UNII: 5M0MWY797U) EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) SODIUM ASCORBATE (UNII: S033EH8359) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CITRAL (UNII: T7EU0O9VPP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10967-620-27 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 Drug M019 01/01/2014 12/31/2024 MITCHUM ADVANCED CONTROL SOLID
aluminum zirconium tetrachlorohydrex gly liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10967-645 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) PPG-14 BUTYL ETHER (UNII: R199TJT95T) TALC (UNII: 7SEV7J4R1U) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) PEG-8 DISTEARATE (UNII: 7JNC8VN07M) .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) COUMARIN (UNII: A4VZ22K1WT) HYDROGEN PEROXIDE (UNII: BBX060AN9V) LIMONENE, (+/-)- (UNII: 9MC3I34447) LINALOOL, (+/-)- (UNII: D81QY6I88E) ISOEUGENOL (UNII: 5M0MWY797U) EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) SODIUM ASCORBATE (UNII: S033EH8359) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CITRAL (UNII: T7EU0O9VPP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10967-645-27 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 Drug M019 01/01/2014 12/31/2024 Labeler - Revlon Consumer Products Corp (788820165) Establishment Name Address ID/FEI Business Operations REVLON, INC. 809725570 manufacture(10967-629, 10967-617, 10967-618, 10967-644, 10967-619, 10967-620, 10967-645)







