FDA.reportPublic FDA data

Speed Stick

Manufacturer
Colgate-Palmolive Company
Effective date
2025-12-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:26:50

Label at a glance#

ProductSpeed Stick Irish Spring Original
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure10 sections

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Tetrachlorohydrex GLY 10.4%

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 - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

OTC - STOP USE SECTION

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.

Directions

DOSAGE & ADMINISTRATION SECTION

apply to underarms only

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients: Elaeis Guineensis (Palm) Kernel Oil, Stearyl Alcohol, Cyclomethicone, C12-15 Alkyl Benzoate, Hydrogenated Castor Oil, PEG-8 Distearate, PPG-14 Butyl Ether, Hydrogenated Soybean Oil, Fragrance, Behenyl Alcohol, Citric Acid, Pentaerythrityl Tetra-Di-T-Butyl Hydroxyhydrocinnamate.

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-228-7408

SPL UNCLASSIFIED SECTION

Dist. by:
COLGATE-PALMOLIVE COMPANY
New York, NY 10022 U.S.A.

PRINCIPAL DISPLAY PANEL - 76 g Container Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SPEED®
STICK

IRISH
SPRING®

ORIGINAL
ANTIPERSPIRANT / DEODORANT

NET WT
27 0Z (76 g)

PS0093218

Principal Display Panel - 76 g Container Label
Principal Display Panel - 76 g Container Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130022200950367GTIN-13: 0022200950367
EAN-13: 0022200950367
GTIN-12: 022200950367
UPC-A: 022200950367
GTIN storage (14 digits): 00022200950367		speedstick-01.jpg
Data codeData Matrix0093219speedstick-01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
35000-774-73Speed StickIrish Spring Original76 g in 1 CONTAINERSTICK762

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
35000-77435000-774-73

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
PALM KERNEL OILB0S90M0233IACT
STEARYL ALCOHOL2KR89I4H1YIACT
CYCLOMETHICONE 50THT5PCI0RIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
PEG-8 DISTEARATE7JNC8VN07MIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
HYDROGENATED SOYBEAN OILA2M91M918CIACT
DOCOSANOL9G1OE216XYIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE)255PIF62MSIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-12-04legacy-cache2026-10-21 17:52:02

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
Speed Stick Irish Spring OriginalALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLYColgate-Palmolive Company6ddfbef4-89ad-4b51-9315-85c8b077153e2025-12-18WarningsExact identifier
ndc (package): 35000-774-73
ndc (product): 35000-774
ndc11 (package): 35000077473
spl id: 7d8da9e5-e25e-41d5-841d-a9c19fe23416
spl set id: 6ddfbef4-89ad-4b51-9315-85c8b077153e

Reported adverse events (FAERS/openFDA)#

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