FDA.reportPublic FDA data

Power Stick Invisible Protection Roll- On Antiperspirant Deodorant Spring Fresh

Manufacturer
A.P. Deauville, LLC
Effective date
2024-07-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:15:20

Label at a glance#

ProductPower Stick Invisible Protection Roll- On Antiperspirant Deodorant Spring Fresh
Active ingredientALUMINUM SESQUICHLOROHYDRATE
Label structure7 sections

Dosage and administration

Apply to underams only.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Sesquichlorohydrate, 25%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm wetness.

Warnings

WARNINGS SECTION

For external ues only.

Do not use

OTC - DO NOT USE SECTION

on broken skin.

Stop use if 

OTC - STOP USE SECTION

rash or irritation occurs

Ask a doctor before use

OTC - ASK DOCTOR SECTION

if you have kidney disease

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately.

Questions?

OTC - QUESTIONS SECTION

(732) 719-3475

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underams only.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, PPG-14 Butyl Ether, Propylene Glycol, Steareth-2, Cyclopentasiloxane, Fragrance, Steareth-21, PEG-8 Distearate, Citric Acid

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42913-039-00Power Stick Invisible Protection Roll- On Antiperspirant Deodorant Spring Fresh53 mL in 1 CONTAINERSTICK533

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42913-039POWER STICK INVISIBLE PROTECTION ROLL- ON ANTIPERSPIRANT DEODORANT SPRING FRESH (ALUMINUM SESQUICHLOROHYDRATE) STICK [A.P. DEAUVILLE, LLC]31 package rows20240716_f6bb8e7f-01b8-4708-a533-bd143cd5a605.zip

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
42913-03942913-039-00

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
WATER059QF0KO0RIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
STEARETH-2V56DFE46J5IACT
CYCLOMETHICONE 50THT5PCI0RIACT
STEARETH-2153J3F32P58IACT
PEG-8 DISTEARATE7JNC8VN07MIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ALUMINUM SESQUICHLOROHYDRATEUCN889409VACTIB

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
5719d227-2f7a-baec-e063-6294a90a5b4df6bb8e7f-01b8-4708-a533-bd143cd5a6052026-07-21WarningsExact identifier
spl set id: f6bb8e7f-01b8-4708-a533-bd143cd5a605

Reported adverse events (FAERS/openFDA)#

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