FDA.reportPublic FDA data

Secret Clinical Strength Soft Light and Fresh

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2023-12-20
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 21:17:26

Label at a glance#

ProductSecret Clinical Strength Soft Light and Fresh
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure10 sections

Dosage and administration

apply to underarms only apply two 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 trichlorohydrex 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 two clicks of product to underarms at bedtime

Inactive ingredients

INACTIVE INGREDIENT SECTION

cyclopentasiloxane, tribehenin, dimethicone, petrolatum, cyclodextrin, fragrance, C18-36 acid triglyceride, PPG-14 butyl ether, panthenyl triacetate

Questions?

OTC - QUESTIONS SECTION

1-800-964-1947

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 73 g Cylinder Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60% MORE

vs 1.6 oz

Secret®

CLINICAL
STRENGTH ®

Soft Solid

light and fresh

Clinically proven prescription strength
wetness protection

ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
ANTIPERSPIRANT/DEODORANT

NET WT. 2.6 OZ. (73 g)

SecretSecret

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69423-13869423-138-45, 69423-138-73, 69423-138-14, 69423-138-01, 69423-138-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
C18-36 ACID TRIGLYCERIDEZRA72DR3R7IACT
CYCLOMETHICONE 50THT5PCI0RIACT
DIMETHICONE92RU3N3Y1OIACT
PETROLATUM4T6H12BN9UIACT
TRIBEHENIN8OC9U7TQZ0IACT
PPG-14 BUTYL ETHERR199TJT95TIACT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB
BETADEXJV039JZZ3AIACT
PANTHENOL TRIACETATE, (+)-1206E8961BIACT

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
0cf91b03-89d2-7bd3-e063-6294a90a7fab40e467df-917b-38ab-e054-00144ff8d46c2023-12-20WarningsExact identifier
spl id: 0cf91b03-89d2-7bd3-e063-6294a90a7fab
spl set id: 40e467df-917b-38ab-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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