FDA.reportPublic FDA data

Mitchum Invisible Solid

Manufacturer
Revlon Consumer Products Corp. | Revlon, INC.
Effective date
2018-10-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:15:20

Label at a glance#

ProductMitchum Invisible Solid
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure9 sections

Indications and uses

Antiperspirant

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Warnings

WARNINGS SECTION

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 irritation 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

DOSAGE & ADMINISTRATION SECTION

Apply to Underarms only

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Tetrachlorohydrex Gly 20%

Inactive Ingredients Section

INACTIVE INGREDIENT SECTION

CYCLOPENTASILOXANE; STEARYL ALCOHOL; C12-15 ALKYL BENZOATE ; PPG-14 BUTYL ETHER; PHENYL TRIMETHICONE; PETROLATUM; HYDROGENATED CASTOR OIL; TALC; PARFUM (FRAGRANCE); SODIUM STARCH OCTENYLSUCCINATE ; LINALOOL; LIMONENE; BENZYL SALICYLATE; HEXYL CINNAMAL; COUMARIN; BENZYL BENZOATE; PEG-40 HYDROGENATED CASTOR OIL; CITRONELLOL; SILICA; GERANIOL

uses

INDICATIONS & USAGE SECTION

Antiperspirant

Mitchum Invisable Solid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aluminum Zirconium Tetrachlorohydrex Gly 20%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

womens curvewomens curvemens curvemens curve

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10967-657-272024-01-12C16284748780-1ba0f9c33-46ec-a910-e053-dadaa90a0b85Mitchum Invisible Solid
10967-657-272021-01-29C16284748780-1ba0f9c33-46ec-a910-e053-dadaa90a0b85Mitchum Invisible Solid

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10967-65710967-657-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYDROXYCITRONELLAL8SQ0VA4YURIACT
PEG-40 CASTOR OIL4ERD2076EFIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
SODIUM ASCORBATES033EH8359IACT
CITRALT7EU0O9VPPIACT
COUMARINA4VZ22K1WTIACT
GERANIOLL837108USYIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
LIMONENE, (+)-GFD7C86Q1WIACT
LINALOOL, (+)-F4VNO44C09IACT
CYCLOMETHICONE 50THT5PCI0RIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
STEARYL ALCOHOL2KR89I4H1YIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
PETROLATUM4T6H12BN9UIACT
TALC7SEV7J4R1UIACT

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
471c97cb-875d-7092-e063-6294a90a6ce9902c7439-7746-3672-e053-2a95a90a5cf62025-12-29WarningsExact identifier
spl set id: 902c7439-7746-3672-e053-2a95a90a5cf6

Reported adverse events (FAERS/openFDA)#

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