FDA.reportPublic FDA data

Secret

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2026-07-28
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
daily-update
Hydrated at
2026-07-31 05:10:23

Label at a glance#

ProductSecret Outlast Completely Clean Invisible Completely Clean
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, PPG-14 butyl ether, C12-15 alkyl benzoate, hydrogenated castor oil, petrolatum, cyclodextrin, fragrance, ozokerite, C20-40 alketh-10, corn starch/maltodextrin crosspolymer, kaolin, behenyl alcohol, bisabolol, panthenyl triacetate, tocopheryl acetate, sodium hyaluronate, zingiber officinale (ginger) root extract

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

Secret®

OUTLAST™

Completely Clean

72 HR INVISIBLE SOLID

ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
ANTIPERSPIRANT/DEODORANT

NET WT. 2.6 OZ (73 g)

SecSec

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130037000808053GTIN-13: 0037000808053
EAN-13: 0037000808053
GTIN-12: 037000808053
UPC-A: 037000808053
GTIN storage (14 digits): 00037000808053		Sec.jpg
Data codeData Matrix20161083Sec.jpg
Data codeData Matrix21443378Sec.jpg

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69423-40569423-405-73, 69423-405-14, 69423-405-96, 69423-405-01, 69423-405-45

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
STEARYL ALCOHOL2KR89I4H1YIACT
MINERAL OILT5L8T28FGPIACT
KAOLIN24H4NWX5COIACT
PETROLATUM4T6H12BN9UIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
C20-40 PARETH-10TE3MZI4V3FIACT
BEHENYL ALCOHOL9G1OE216XYIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
CYCLODEXTRIN7E6SK9QDT8IACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
CERESINQ1LS2UJO3AIACT
BISABOLOL24WE03BX2TIACT
PANTHENYL TRIACETATE1206E8961BIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
SODIUM HYALURONATEYSE9PPT4THIACT
GINGERC5529G5JPQIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52025-11-24full-release2026-06-01 01:17:58

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
Secret Outlast Completely Clean Invisible Completely CleanALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLYThe Procter & Gamble Manufacturing Companyf4382fa6-a8c6-5e00-e053-2995a90a7e512026-07-28WarningsExact identifier
ndc (package): 69423-405-96
ndc (package): 69423-405-01
ndc (package): 69423-405-45
ndc (package): 69423-405-73
ndc (package): 69423-405-14
ndc (product): 69423-405
ndc11 (package): 69423040596
ndc11 (package): 69423040514
ndc11 (package): 69423040573
ndc11 (package): 69423040545
ndc11 (package): 69423040501
spl id: 57b11e08-4b6f-db4b-e063-6294a90a8af8
spl set id: f4382fa6-a8c6-5e00-e053-2995a90a7e51

Reported adverse events (FAERS/openFDA)#

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