POWER UP

Manufacturer: VVF Kansas Services LLC
Effective date: 2021-11-17
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 22:26:50

Label at a glance#

ProductPOWER UP DRIVE

Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY

Label structure13 sections

Indications and uses

reduces underarm wetness

Dosage and administration

Apply to underarms only

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Trichlorohydrex GLY 19%

Purpose

OTC - PURPOSE SECTION

anti-perspirant

Uses

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 doctor before use if you have kidney disease

OTC - STOP USE SECTION

Stop use if rash or irritation occurs

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only

Other information

SPL UNCLASSIFIED SECTION

Do not store over 115 °F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, Stearyl Alcohol *, Mineral Oil,

Hydrogenated Castor Oil, Fragrance, C12-15 Alkyl

Benzoate, PPG-14 Butyl Ether, Phenyl Trimethicone,

Glyceryl Stearate, Talc, PEG-100 Stearate, Behenyl

Alcohol *.

SPL UNCLASSIFIED SECTION

*These are waxes and are not derived from liquid alcohol nor are they flammable.

Alcohol Free

Distributed by:

Olivette Products, L.L.C., Bridgeton, MO 63044

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Power Up Drive AP Labels

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

POWER UP DRIVE
Aluminum Zirconium Trichlorohydrex GLY 19%
CYCLOMETHICONE 5
STEARYL ALCOHOL
MINERAL OIL
PPG-14 BUTYL ETHER
GLYCERYL STEARATE SE
TALC
HYDROGENATED CASTOR OIL
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
ALKYL (C12-15) BENZOATE
PHENYL TRIMETHICONE
PEG-100 STEARATE
DOCOSANOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10889-410	10889-410-01

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
Name	UNII	Kind
CYCLOMETHICONE 5	0THT5PCI0R	IACT
STEARYL ALCOHOL	2KR89I4H1Y	IACT
MINERAL OIL	T5L8T28FGP	IACT
PPG-14 BUTYL ETHER	R199TJT95T	IACT
GLYCERYL STEARATE SE	FCZ5MH785I	IACT
TALC	7SEV7J4R1U	IACT
HYDROGENATED CASTOR OIL	ZF94AP8MEY	IACT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY	T27D6T99LH	ACTIB
ALKYL (C12-15) BENZOATE	A9EJ3J61HQ	IACT
PHENYL TRIMETHICONE	DR0K5NOJ4R	IACT
PEG-100 STEARATE	YD01N1999R	IACT
DOCOSANOL	9G1OE216XY	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
d0fd9436-14b1-063a-e053-2a95a90ae454			46b02e1f-2e60-4df9-92f4-5dc055c581a4	2021-11-17	Warnings	Exact identifier spl id: d0fd9436-14b1-063a-e053-2a95a90ae454 spl set id: 46b02e1f-2e60-4df9-92f4-5dc055c581a4

Reported adverse events (FAERS/openFDA)#

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