FDA.reportPublic FDA data

Antiperspirant Lotion for Hands Feet Body Zero Sweat ®

Manufacturer
Zero Sweat Inc. | BMC 1092, Inc. dba Solo Laboratories, Inc
Effective date
2020-01-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:30:52

Label at a glance#

ProductAntiperspirant for Hands Feet Body Zero Sweat
Active ingredientAluminum Sesquichlorohydrate
Label structure10 sections

Indications and uses

Treats Excessive Perspiration

Dosage and administration

Wash and dry area thoroughly before application Apply a small amount Rub in vigorously for a minimum of 15 Allow time to air dry

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Sesquichlorohydrate

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

  • Treats Excessive Perspiration

Warnings

WARNINGS SECTION

For external use only

Do Not Use

OTC - DO NOT USE SECTION

on irritated skin

  • On irritated skin

OTC - STOP USE SECTION

Stop use and ask a doctor if rash or irritation develops

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

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

  • Wash and dry area thoroughly before application
  • Apply a small amount
  • Rub in vigorously for a minimum of 15
  • Allow time to air dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,Steareth-2, Aluminum Starch Octenyl Succinate, Steareth-20, PPG-15 Stearyl Ether, Isopropyl Myristate, Dimethicone

Questions?

OTC - QUESTIONS SECTION

Email dry@zerosweat.com

PRINCIPAL DISPLAY PANEL - 40 ml Tube Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZERO Z SWEAT®

Keeps You Dry.

Antiperspirant
Lotion

For Hands, Feet, Body

1.35 FL. OZ. (40 ml.)

Principal Display Panel - 40 ml Tube Box
Principal Display Panel - 40 ml Tube Box

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55726-293-402024-01-30C16284748780-19d75b9d0-e4b5-f424-e053-dadaa90a57ceAntiperspirant Lotion for Hands Feet Body Zero Sweat ®
55726-293-402020-10-02C16284748780-19d75b9d0-e4b5-f424-e053-dadaa90a57ceAntiperspirant Lotion for Hands Feet Body Zero Sweat ®
55726-293-402020-01-31C16284748780-19d75b9d0-e4b5-f424-e053-dadaa90a57ceAntiperspirant Lotion for Hands Feet Body Zero Sweat ®

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55726-293-40Antiperspirant for Hands Feet Body Zero Sweat40 mL in 1 TUBELOTION402
55726-293-40Antiperspirant for Hands Feet Body Zero Sweat1 in 1 BOX, UNIT-DOSELOTION12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55726-293ANTIPERSPIRANT FOR HANDS FEET BODY ZERO SWEAT (ALUMINUM SESQUICHLOROHYDRATE) LOTION [ZERO SWEAT INC.]2Legacy NDC, 2 package rows20201003_9c3f9b2e-590a-4a73-a037-c5ba871d5b88.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55726-29355726-293-40

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
Aluminum SesquichlorohydrateUCN889409VACTIB
Water059QF0KO0RIACT
Steareth-2V56DFE46J5IACT
Aluminum starch OctenylsuccinateI9PJ0O6294IACT
Steareth-20L0Q8IK9E08IACT
PPG-15 Stearyl Ether1II18XLS1LIACT
Isopropyl Myristate0RE8K4LNJSIACT
Dimethicone92RU3N3Y1OIACT

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
889f39b3-63d9-4ac0-8629-556b7ba63e739c3f9b2e-590a-4a73-a037-c5ba871d5b882020-01-10WarningsExact identifier
spl id: 889f39b3-63d9-4ac0-8629-556b7ba63e73
spl set id: 9c3f9b2e-590a-4a73-a037-c5ba871d5b88

Reported adverse events (FAERS/openFDA)#

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