Anti-Perspirant Deodorant

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 20:43:55

Label at a glance#

ProductAnti-Perspirant Deodorant
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure12 sections

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminium Zirconium Tetrachlorohydrex Gly (15%)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

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 Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Brassica Glycerides, Polyester-4, C 13-16 lsoparaffin, Heptyl Undecylenate, Cyclotetrasiloxane. Caprylic/Capric Triglyceride, PPG-14 Butyl Ether, Stearyl Alcohol, Fragrance

Questions or comments?

OTC - QUESTIONS SECTION

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

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59 mL in Bottle; NDC 74553-001-01

DeoDeo

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74553-00174553-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
7907ae4c-472a-4414-9ec6-8b620719ca48b0fdfe63-fee8-9f79-e053-2a95a90ac30f2025-03-12WarningsExact identifier
spl set id: b0fdfe63-fee8-9f79-e053-2a95a90ac30f

Reported adverse events (FAERS/openFDA)#

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