FDA.reportPublic FDA data

Secret

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2026-06-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
daily-update
Hydrated at
2026-06-16 05:10:19

Label at a glance#

ProductSecret Clinical Clear Completely Clean
Active ingredientALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY
Label structure10 sections

Dosage and administration

apply to underarms only apply 2-3 clicks of product to underarms at bedtime

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum zirconium octachlorohydrex Gly 20% (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
  • apply 2-3 clicks of product to underarms at bedtime

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cyclopentasiloxane, dimethicone, propylene glycol, alcohol denat., calcium chloride, bisabolol, zingiber officinale (ginger) root extract, tocopheryl acetate, panthenyl triacetate, PEG/PPG-18/18 dimethicone, fragrance

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 45 g Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100 HR PROTECTION

Secret

CLINICAL

COMPLETELY CLEAN

CLEAR GEL

ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY
ANTIPERSPIRANT / DEODORANT

NET WT. 1.6 OZ (73 g)

SECSEC

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix21354803SEC.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

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
69423-69369423-693-45, 69423-693-73

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
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
GINGERC5529G5JPQIACT
BISABOLOL24WE03BX2TIACT
ALCOHOL3K9958V90MIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
DIMETHICONE92RU3N3Y1OIACT
CALCIUM CHLORIDEM4I0D6VV5MIACT
PEG/PPG-18/18 DIMETHICONE9H0AO7T794IACT
ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLYP9D3YP29MYACTIB
PANTHENYL TRIACETATE1206E8961BIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32025-12-31full-release2026-06-01 01:30:54

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 Clinical Clear Completely CleanALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLYThe Procter & Gamble Manufacturing Companyf792c584-692e-8990-e053-6394a90a6cb52026-06-11WarningsExact identifier
ndc (package): 69423-693-73
ndc (package): 69423-693-45
ndc (product): 69423-693
ndc11 (package): 69423069373
ndc11 (package): 69423069345
spl id: 5400894f-fc65-cac7-e063-6394a90a16f6
spl set id: f792c584-692e-8990-e053-6394a90a6cb5

Reported adverse events (FAERS/openFDA)#

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