FDA.reportPublic FDA data

Okay Mens Aluminium Free Deodorant Stick

Manufacturer
Xtreme Tools International, Inc
Effective date
2024-12-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:43:59

Label at a glance#

ProductOkay Mens Aluminium Free Deodorant Stick
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure13 sections

Indications and uses

Reduces underarm wetness.

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Tetrachlorohydrex GLY (20%)………………….................Purpose: Antiperspirant

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

Reduces underarm wetness.

Warnings

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on broken skin.

OTC - STOP USE SECTION

Stop Use and ask doctor if Rash or irritation occurs.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If swallowed get medical help, or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane,Cetearyl Alcohol, PPG-14-Butyl Ether, HydroxypropylStarch Phosphate, Propylene Glycol, Glyceryl Stearate, PEG-100 Stearate, Myristyl Myristate, Silica Dimethyl Silylate, Cetyl Ricinoleate, PEG-40-Hydrogenated Castor Oil, Fragrance.

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-305-622-7474 Monday-Friday 9:00 AM to 5:00 PM

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

56 gr (2oz) in Twist up Tube (NDC 74553-010-01)

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Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

85 gr (3oz) in Twist up Tube (NDC 74553-010-02)

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Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74553-01074553-010-01, 74553-010-02

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
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
HYDROXYPROPYL DISTARCH PHOSPHATE, HIGH AMYLOSE CORN9F8ET54T05IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
MYRISTYL MYRISTATE4042ZC00DYIACT
SILICA DIMETHYL SILYLATEEU2PSP0G0WIACT
CETYL RICINOLEATE1P677500YDIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT

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
3be2fcda-8e59-4f30-9744-06f8fdf2832ad674c832-1ee5-488c-a4b4-477eab04f1bc2025-03-13WarningsExact identifier
spl set id: d674c832-1ee5-488c-a4b4-477eab04f1bc

Reported adverse events (FAERS/openFDA)#

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