FDA.reportPublic FDA data

Secret Invisible Mountain Spring

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2023-03-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:35:01

Label at a glance#

ProductSecret Invisible Mountain Spring
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX 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 pentachlorohydrex GLY 18% (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, petrolatum, hydrogenated castor oil, PPG-14 butyl ether, fragrance, cyclodextrin, behenyl alcohol

Questions?

OTC - QUESTIONS SECTION

1-800-964-1947

SPL UNCLASSIFIED SECTION

Dist. by Procter & Gamble, Cincinnati, OH 45202.

PRINCIPAL DISPLAY PANEL - 73 g Container Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

pH Balanced

Secret ®

Mountain Spring

24 HR INVISIBLE SOLID

Aluminum zirconium pentachlorohydres gly

Antiperspirant / Deodorant

Net Wt. 2.6 OZ (73 g)

SecSec

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
69423-66369423-663-73

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
BETADEXJV039JZZ3AIACT
CYCLOMETHICONE 50THT5PCI0RIACT
STEARYL ALCOHOL2KR89I4H1YIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
MINERAL OILT5L8T28FGPIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
PETROLATUM4T6H12BN9UIACT
DIMETHICONE92RU3N3Y1OIACT
DOCOSANOL9G1OE216XYIACT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB

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
288b52ed-ed04-96e6-e063-6394a90aa254f656d9b2-061a-247c-e053-2a95a90a7f342024-12-05WarningsExact identifier
spl set id: f656d9b2-061a-247c-e053-2a95a90a7f34

Reported adverse events (FAERS/openFDA)#

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