Secret Clinical Dry Spray Light and Fresh

Manufacturer: The Procter & Gamble Manufacturing Company
Effective date: 2025-10-29
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:41:17

Label at a glance#

ProductSecret Clinical Dry Light and Fresh

Active ingredientALUMINUM SESQUICHLOROHYDRATE

Label structure10 sections

Dosage and administration

apply to underarms only

Contacts and useful links#

PhoneLabel contact1-800-964-1947

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum sesquichlorohydrate 24.7.0% (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.

SPL UNCLASSIFIED SECTION

Flammable

do not spray near flame or while smoking

contents under pressure

do not crush, puncture or incinerate

do not expose to heat or store at temperature above 120ºF

OTC - WHEN USING SECTION

When using this product

keep away from face and mouth to avoid breathing it

avoid spraying in eyes

use only as directed; intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal

Directions

DOSAGE & ADMINISTRATION SECTION

apply to underarms only

Inactive ingredients

INACTIVE INGREDIENT SECTION

Butane, cyclopentasiloxane, hydrofluorocarbon 152A, fragrance, disteardimonium hectorite, dimethicone, propylene carbonate, dimethiconol

SPL UNCLASSIFIED SECTION

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

Questions or comments?

OTC - QUESTIONS SECTION

1-800-964-1947

PRINCIPAL DISPLAY PANEL - 107 g Can

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Secret ®

CLINICAL

DRY SPRAY

LIGHT & FRESH

ALUMINUM SESQUICHLOROHYDRATE

ANTIPERSPIRANT/DEODORANT

NET WT. 3.8 OZ (107 g)

SEC

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Data code	Data Matrix	21102796		SEC.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84126-185-10	Secret Clinical Dry Light and Fresh	107 g in 1 CAN	AEROSOL, SPRAY	107		1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Secret Clinical Dry Light and Fresh
Aluminum sesquichlorohydrate
BUTANE
DISTEARDIMONIUM HECTORITE
DIMETHICONE
DIMETHICONOL (100000 CST)
PROPYLENE CARBONATE
CYCLOPENTASILOXANE
HYDROFLUOROCARBON 152A

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84126-185	84126-185-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BUTANE	6LV4FOR43R	IACT
DISTEARDIMONIUM HECTORITE	X687XDK09L	IACT
DIMETHICONE	92RU3N3Y1O	IACT
ALUMINUM SESQUICHLOROHYDRATE	UCN889409V	ACTIB
DIMETHICONOL (100000 CST)	OSA9UP217S	IACT
PROPYLENE CARBONATE	8D08K3S51E	IACT
CYCLOPENTASILOXANE	0THT5PCI0R	IACT
HYDROFLUOROCARBON 152A	0B1U8K2ME0	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Secret Clinical Dry Light and Fresh	ALUMINUM SESQUICHLOROHYDRATE	The Procter & Gamble Manufacturing Company	424dac04-72e1-028d-e063-6294a90a6ee4	2025-10-29	Warnings	Exact identifier ndc (package): 84126-185-10 ndc (product): 84126-185 ndc11 (package): 84126018510 spl id: 424dabdc-e530-c312-e063-6394a90a754e spl set id: 424dac04-72e1-028d-e063-6294a90a6ee4

Reported adverse events (FAERS/openFDA)#

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