FDA.reportPublic FDA data

Revlon Mitchum Clinical Gel

Manufacturer
Revlon Consumer Products Corp | REVLON, INC.
Effective date
2024-12-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:49:53

Label at a glance#

ProductRevlon Mitchum Clinical Gel
Active ingredientALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Octachlorohydrex Gly 20%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Aqua ((Water) Eau), Alcohol Denat., Cyclopentasiloxane, Dimethicone, Dipropylene Glycol, PEG/PPG-18/18 Dimethicone, Parfum (Fragrance), Citronellol, Cinnamal, Coumarin, Geraniol

INDICATIONS & USAGE SECTION

Reduces underarm wetness

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCartonMitchum Roll On

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10967-632-02Revlon Mitchum Clinical Gel59 mL in 1 CONTAINERLIQUID593
10967-633-02Revlon Mitchum Clinical Gel59 mL in 1 CONTAINERLIQUID593
10967-633-60Revlon Mitchum Clinical Gel17 mL in 1 CONTAINERLIQUID173

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10967-632REVLON MITCHUM CLINICAL GEL (ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY LIQUID) LIQUID [REVLON CONSUMER PRODUCTS CORP]3Current NDC, Legacy NDC, 1 package rows20250101_43287217-d0ad-3229-e054-00144ff88e88.zip
10967-633REVLON MITCHUM CLINICAL GEL (ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY LIQUID) LIQUID [REVLON CONSUMER PRODUCTS CORP]3Current NDC, Legacy NDC, 2 package rows20250101_43287217-d0ad-3229-e054-00144ff88e88.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10967-63210967-632-02
10967-63310967-633-02, 10967-633-60

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
DIMETHICONE92RU3N3Y1OIACT
PEG/PPG-18/18 DIMETHICONE9H0AO7T794IACT
COUMARINA4VZ22K1WTIACT
DIPROPYLENE GLYCOLE107L85C40IACT
CYCLOMETHICONE 50THT5PCI0RIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
GERANIOLL837108USYIACT
ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLYP9D3YP29MYACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
DIMETHICONE92RU3N3Y1OIACT
PEG/PPG-18/18 DIMETHICONE9H0AO7T794IACT
COUMARINA4VZ22K1WTIACT
DIPROPYLENE GLYCOLE107L85C40IACT
CYCLOMETHICONE 50THT5PCI0RIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
GERANIOLL837108USYIACT
ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLYP9D3YP29MYACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Revlon Mitchum Clinical GelALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY LIQUIDRevlon Consumer Products Corp43287217-d0ad-3229-e054-00144ff88e882024-12-31WarningsExact identifier
ndc (package): 10967-633-60
ndc (package): 10967-632-02
ndc (package): 10967-633-02
ndc (product): 10967-632
ndc (product): 10967-633
ndc11 (package): 10967063302
ndc11 (package): 10967063360
ndc11 (package): 10967063202
spl id: 2a968ae6-b455-db91-e063-6294a90a4022
spl set id: 43287217-d0ad-3229-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.