FDA.reportPublic FDA data

SWEATBLOCK

Manufacturer
DC Alpine Partners, LLC
Effective date
2022-01-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:19:43

Label at a glance#

ProductSWEATBLOCK
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure11 sections

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

Deodorant

SPL UNCLASSIFIED SECTION

+ Motion-activated antiperspirant

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminium Zirconium Tetrachlorohydrex Gly (15.2%)

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

Questions?

OTC - QUESTIONS SECTION

Call toll free 1-855-796-2566

Scan with Transparency App

SPL UNCLASSIFIED SECTION

Distributed by:

SweatBlock

Alpine, UT 84004, USA

855-796-2566

www.sweatblock.com

SWEATBLOCK Odor Series

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Deodorant

+ Motion-activated antiperspirant

Up to 24 hours 24 Odor protection

Net wt 2.7 oz (76 g)

SweatBlock Deodorant + Motion-Activated Antiperspirant Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SweatBlock Deodorant BackSweatBlock Deodorant BackSweatBlock Deodorant FrontSweatBlock Deodorant Front

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
54913-15254913-152-76

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
NameUNIIKind
STEARYL ALCOHOL2KR89I4H1YIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
PEG-8 DISTEARATE7JNC8VN07MIACT
CYCLOMETHICONE 50THT5PCI0RIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
PPG-14 BUTYL ETHERR199TJT95TIACT

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
d4807a52-d413-07cc-e053-2995a90a53e09b02afd7-4a82-7773-e053-2a95a90ab8812022-01-01WarningsExact identifier
spl id: d4807a52-d413-07cc-e053-2995a90a53e0
spl set id: 9b02afd7-4a82-7773-e053-2a95a90ab881

Reported adverse events (FAERS/openFDA)#

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