FDA.reportPublic FDA data

Aramis Antiperspirant

Manufacturer
KDC/one Swallowfield Limited
Effective date
2020-02-24
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:40:22

Label at a glance#

ProductAramis Antiperspirant
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient                                                    Purpose

Aluminum Zirconium Tetrachlorohydrex GLY            Antiperspirant

OTC - PURPOSE SECTION

Uses

decreases underarm Perspiration

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

INDICATIONS & USAGE SECTION

Ask a doctor before use if you have Kidney Disease

WARNINGS SECTION

Warnings

For External Use only

Do not use on Broken Skin

Ask a doctor before use if you have kidney disease

DOSAGE & ADMINISTRATION SECTION

Directions

Apply to underarms only

INACTIVE INGREDIENT SECTION

Inactive ingredients​: Cyclopentasiloxane, Stearyl alcohol, Talc, PPG-14 Butyl Ether, Hydrogenated, Arachidyl Alcohol, Fragrance (Parfum), Lauryl Methacrylate/Glycol Dimethacrylate Crosspolymer, Limonene, Hexy Cinnamal, Alpha-Isomethyl Isonone, Geraniol, Hydroxycitronellal, Eugenol, Linalool, Citronellol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aramis

"24 HOUR"

High Performance

Antiperspirant Stick

Stick Antiperspirant

Poids Net Wt. 2.6 Oz./75 ml

PrimaryPrimary

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50503-001-022020-02-24C16284748780-19d75b9d0-c7e4-f424-e053-dadaa90a57ceAramis Antiperspirant Stick
50503-001-022020-01-31C16284748780-19d75b9d0-c7e4-f424-e053-dadaa90a57ceAramis Antiperspirant Stick

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50503-00150503-001-01, 50503-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
STEARYL ALCOHOL2KR89I4H1YIACT
TALC7SEV7J4R1UIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
ARACHIDYL ALCOHOL1QR1QRA9BUIACT
LAURYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMEREX0F4CZ66HIACT
LIMONENE, (+)-GFD7C86Q1WIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
GERANIOLL837108USYIACT
HYDROXYCITRONELLAL8SQ0VA4YURIACT
EUGENOL3T8H1794QWIACT
LINALOOL, (+)-F4VNO44C09IACT
.BETA.-CITRONELLOL, (+/-)-565OK72VNFIACT

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
f05e370f-3fa0-4cc8-e053-2995a90ac99cd7e49e5e-690e-425e-9932-9c7e7d63d0492022-12-21WarningsExact identifier
spl set id: d7e49e5e-690e-425e-9932-9c7e7d63d049

Reported adverse events (FAERS/openFDA)#

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