FDA.reportPublic FDA data

ART OF SPORT ANTIPERSPIRANT plus DEODORANT CHALLENGE

Manufacturer
AOS Group, INC.
Effective date
2021-03-10
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:49:22

Label at a glance#

ProductART OF SPORT ANTIPERSPIRANT plus DEODORANT CHALLENGE
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Aluminum Zirconium Tetrachlorohydrex Gly (15.2%)

OTC - PURPOSE SECTION

Purpose
Antiperspirant

INDICATIONS & USAGE SECTION

Uses
reduces underarm wetness

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 irritation occurs

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

DOSAGE & ADMINISTRATION SECTION

Directions
apply to underarms only

INACTIVE INGREDIENT SECTION

Inactive Ingredients
Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, Fragrance, Hydrogenated Castor Oil, Silica, Isorpropyl Myristate, PEG-8 Distearate, Glycerin, Maranta Arundinacea Root Extract, Camellia Sinensis Leaf Extract

OTC - QUESTIONS SECTION

Questions?
Call 1-503-610-4055
help@artofsport.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Art of Sport - Antiperspirant-Deodorant - ChallengeArt of Sport - Antiperspirant-Deodorant - Challenge

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72698-301-112021-03-10C16284748780-1ba0f9c33-135c-a910-e053-dadaa90a0b85Antiperspirant/deodorant. Re-doing the Challenge version, with a newly generated Set ID
72698-301-112021-01-29C16284748780-1ba0f9c33-135c-a910-e053-dadaa90a0b85Antiperspirant/deodorant. Re-doing the Challenge version, with a newly generated Set ID

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
72698-30172698-301-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
CYCLOMETHICONE 50THT5PCI0RIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
GLYCERINPDC6A3C0OXIACT
MARANTA ARUNDINACEA ROOTFVN346W31AIACT
STEARYL ALCOHOL2KR89I4H1YIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
PPG-14 BUTYL ETHERR199TJT95TIACT
PEG-8 DISTEARATE7JNC8VN07MIACT

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
d5f783f4-7303-8541-e053-2a95a90a06bb8df9d658-742a-5f69-e053-2995a90a020f2022-01-19WarningsExact identifier
spl set id: 8df9d658-742a-5f69-e053-2995a90a020f

Reported adverse events (FAERS/openFDA)#

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