FDA.reportPublic FDA data

Mitchum Sensitive Skin

Manufacturer
Revlon Consumer Products Corp | REVLON, INC.
Effective date
2019-11-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:01:57

Label at a glance#

ProductMitchum Sensitive Skin
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure8 sections

Dosage and administration

Apply to underarms only

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Tetrachlorohydrex 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

Keep out of reach of children

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

Cyclopentasiloxane, Stearyl Alcohol, Isopropyl Myristate, Dimethicone, Hydrogenated Castor Oil, Talc, Petrolatum, PEG-23 Glyceryl Distearate, Aloe Barbadensis Leaf Extract, Allantoin, Tocopheryl Acetate

INDICATIONS & USAGE SECTION

Reduces underarm wetness

Directions

INSTRUCTIONS FOR USE SECTION

Apply to underarms only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mitchum Sensitive

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10967-634-272024-01-12C16284748780-1ba0f9c33-2a22-a910-e053-dadaa90a0b85Mitchum Sensitive Skin
10967-634-272021-01-29C16284748780-1ba0f9c33-2a22-a910-e053-dadaa90a0b85Mitchum Sensitive Skin

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10967-63410967-634-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
CYCLOMETHICONE 50THT5PCI0RIACT
STEARYL ALCOHOL2KR89I4H1YIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
DIMETHICONE92RU3N3Y1OIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
TALC7SEV7J4R1UIACT
PETROLATUM4T6H12BN9UIACT
PEG-23 GLYCERYL DISTEARATE527412VE0UIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALLANTOIN344S277G0ZIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB

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
0ec85c68-00cb-405e-e063-6394a90a1ea8432cbf25-d054-63f3-e054-00144ff8d46c2024-01-12WarningsExact identifier
spl set id: 432cbf25-d054-63f3-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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