SWEATBLOCK

Manufacturer: DC Alpine Partners, LLC
Effective date: 2022-01-01
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 22:19:49

Label at a glance#

ProductSWEATBLOCK

Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY

Label structure11 sections

Dosage and administration

Apply to underarms only.

Contacts and useful links#

PhoneLabel contact1-855-796-2566

Websitewww.sweatblock.com

www.sweatblock.com

Label contents#

Full prescribing information#

CLINICAL PROTECTION

SPL UNCLASSIFIED SECTION

Deodorant + Antiperspirant

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Tetrachlorohydrex Gly (20%)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm wetness

Warnings

WARNINGS SECTION

For external use 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 if

OTC - ASK DOCTOR SECTION

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 Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, Fragrance, Hydrogenated Castor Oil, Isopropyl Myristate, PEG-8 Distearate, PPG-14 Butyl Ether, Silica, Stearyl Alcohol

Questions?

OTC - QUESTIONS SECTION

Call toll free 1-855-796-2566

Distributed by:

SPL UNCLASSIFIED SECTION

SweatBlock

Alpine, UT 84004, USA

855-796-2566

www.sweatblock.com

CLINICAL PROTECTION

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SWEATBLOCK

COASTAL FRESH

Deodorant +

Antiperspirant

HOUR

SweatBlock Clinical Antiperspirant & Deodorant Solid Labels.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label frontLabel back

Products#

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

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

SWEATBLOCK
Aluminum Zirconium Tetrachlorohydrex Gly
PEG-8 DISTEARATE
PPG-14 BUTYL ETHER
SILICON DIOXIDE
CYCLOMETHICONE 5
STEARYL ALCOHOL
HYDROGENATED CASTOR OIL
ISOPROPYL MYRISTATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
54913-020	54913-020-76

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
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	8O386558JE	ACTIB
PEG-8 DISTEARATE	7JNC8VN07M	IACT
PPG-14 BUTYL ETHER	R199TJT95T	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
CYCLOMETHICONE 5	0THT5PCI0R	IACT
STEARYL ALCOHOL	2KR89I4H1Y	IACT
HYDROGENATED CASTOR OIL	ZF94AP8MEY	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	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
d4808298-2e66-4d88-e053-2995a90afb78			bb27c000-19e9-39ae-e053-2a95a90a2180	2022-01-01	Warnings	Exact identifier spl id: d4808298-2e66-4d88-e053-2995a90afb78 spl set id: bb27c000-19e9-39ae-e053-2a95a90a2180

Reported adverse events (FAERS/openFDA)#

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