MITCHUM ULTIMATE- 72 HOUR PROTECTION - WILD ENERGY SOLID - APDEO- antiperspirant and deodorant stick

Mitchum Ultimate- 72 hour protection - Wild Energy Solid - APDEO by

Drug Labeling and Warnings

Mitchum Ultimate- 72 hour protection - Wild Energy Solid - APDEO 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

Uses

Reduces underam wetness

Warnings

For external use only.

Do Not Use

Do not use on broken skin.

Stop Use

Stop use if rash or irritation occurs.

Ask a doctor

Ask a doctor before use if you have kidney disease.

Keep out of reach of children

Keep out of reach of children, if swallowed, seek medical attention or conduct a poison center right away.

Directions

Directions Apply to underarms only.

Inactive ingredients

Cyclopentasiloxane, Stearyl Alcohol, C12-15 Alkyl Benzoate, PPG-14 Butyl Ether, Phenyl Trimethicone, Petrolatum, Hydrogenated Castor Oil, Parfum (Fragrance), Talc, BHT, Calcium Disodium EDTA, Citric Acid, Hydrated Silica, Mannitol, Sodium Ascorbate, Sodium Starch Octenylsuccinate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MITCHUM ULTIMATE- 72 HOUR PROTECTION - WILD ENERGY SOLID - APDEO 
antiperspirant and deodorant stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-790
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	20.2 g  in 76 g

Inactive Ingredients
Ingredient Name	Strength
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
PETROLATUM (UNII: 4T6H12BN9U)
CALCIUM DISODIUM EDTA (UNII: 8U5D034955)
MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
MANNITOL (UNII: 3OWL53L36A)
CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
CITRIC ACID (UNII: 2968PHW8QP)
TALC (UNII: 7SEV7J4R1U)
BHT (UNII: 1P9D0Z171K)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
SODIUM ASCORBATE (UNII: S033EH8359)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-790-27	76 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	10/17/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	10/17/2025

Labeler - Revlon Consumer Products Corp. (788820165)

Registrant - Revlon, Inc. (188442578)

Establishment
Name	Address	ID/FEI	Business Operations
Revlon, Inc.		809725570	manufacture(10967-790)