Label: MITCHUM CLINICAL SOFT SOLID- aluminum zirconium tetrachlorohydrex gly 20.0% gel
- NDC Code(s): 10967-658-16
- Packager: Revlon Consumer Products Corp.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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Drug Label Information
Updated January 1, 2019
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- Official Label (Printer Friendly)
- Active Ingredients
- Keep out of reach of children
-
Inactive Ingredient section
Cyclopentasiloxane; Tribehenin; DIimethicone; Petrolatum; Parfume (Fragrance); Trisiloxane; C18-36 Acid Triglyceride; Aloe Barbadensis Leaf Extract; Tocopheryl Acetate; Sodium Starch Octenylsuccinate, Citric Acid, BHT, Sodium Ascorbate,
Calcium Disodium EDTA, Hydrated Silica, Hexyl Cinnamal, Limonene, Linalool, Mannitol,
Benzyl Salicylate, Alpha-Isomethyl Ionone, Citronellol, Hydroxycitronellal, Benzyl Benzoate,
Geraniol, Cinnamyl Alcohol.
- Uses
- DOSAGE & ADMINISTRATION
- WARNINGS
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MITCHUM CLINICAL SOFT SOLID
aluminum zirconium tetrachlorohydrex gly 20.0% gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10967-658 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 g Inactive Ingredients Ingredient Name Strength CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) TRISILOXANE (UNII: 9G1ZW13R0G) WATER (UNII: 059QF0KO0R) MANNITOL (UNII: 3OWL53L36A) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) DIMETHICONE (UNII: 92RU3N3Y1O) PETROLATUM (UNII: 4T6H12BN9U) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955) COUMARIN (UNII: A4VZ22K1WT) SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B) HYDRATED SILICA (UNII: Y6O7T4G8P9) HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q) BENZYL SALICYLATE (UNII: WAO5MNK9TU) GERANIOL (UNII: L837108USY) CINNAMALDEHYDE (UNII: SR60A3XG0F) METHYL HEPTINE CARBONATE (UNII: 0TTP6YT2T3) LIMONENE, (+)- (UNII: GFD7C86Q1W) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) BENZYL BENZOATE (UNII: N863NB338G) EUGENOL (UNII: 3T8H1794QW) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) SODIUM ASCORBATE (UNII: S033EH8359) LINALOOL, (+)- (UNII: F4VNO44C09) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) CITRAL (UNII: T7EU0O9VPP) HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR) .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418) TRIBEHENIN (UNII: 8OC9U7TQZ0) C18-36 ACID TRIGLYCERIDE (UNII: ZRA72DR3R7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10967-658-16 45 g in 1 CANISTER; Type 0: Not a Combination Product 10/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 10/01/2018 Labeler - Revlon Consumer Products Corp. (788820165) Establishment Name Address ID/FEI Business Operations REVLON, INC. 809725570 manufacture(10967-658)