FDA.reportPublic FDA data

Secret Outlast Xtend Technology Invisible

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2020-01-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:43:44

Label at a glance#

ProductSecret Outlast Xtend Technology Invisible Unscented
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 19% (anhydrous)

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

cyclopentasiloxane, stearyl alcohol, mineral oil, dimethicone, talc, petrolatum, cyclodextrin, hydrogenated castor oil, PPG-14 butyl ether, C20-40 pareth-10, behenyl alcohol, fragrance 1

1 masking fragrance

Questions?

OTC - QUESTIONS SECTION

1-800-964-1947

SPL UNCLASSIFIED SECTION

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202.

PRINCIPAL DISPLAY PANEL - 73 g Cylinder Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INVISIBLE SOLID

Secret®

OUTLAST™

xtend
TECHNOLOGY™

unscented

ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
ANTIPERSPIRANT/DEODORANT

NET WT. 2.6 OZ (73 g)

97548459

Principal Display Panel - 73 g Cylinder Label
Principal Display Panel - 73 g Cylinder Label

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69423-08469423-084-73

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
STEARYL ALCOHOL2KR89I4H1YIACT
MINERAL OILT5L8T28FGPIACT
DIMETHICONE92RU3N3Y1OIACT
TALC7SEV7J4R1UIACT
PETROLATUM4T6H12BN9UIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
C20-40 PARETH-10TE3MZI4V3FIACT
DOCOSANOL9G1OE216XYIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB

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
9cc1e7e2-2a46-4e8c-e053-2a95a90a8fc8869414f0-8acf-4889-b516-e9f18d71b8772020-01-22WarningsExact identifier
spl id: 9cc1e7e2-2a46-4e8c-e053-2a95a90a8fc8
spl set id: 869414f0-8acf-4889-b516-e9f18d71b877

Reported adverse events (FAERS/openFDA)#

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