FDA.reportPublic FDA data

Antiperspirant

Manufacturer
Blue Cross Labs | Zhejiang Greenface Housewares Co.,Ltd
Effective date
2018-12-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:57:52

Label at a glance#

ProductAntiperspirant Maximum Security
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Purpose

Aluminum Zirconium tetrachlorohydrex Gly 8.6% W/W Antiperspirant

OTC - PURPOSE SECTION

Use reduces underarm perspiration

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.

INDICATIONS & USAGE SECTION

Stop use and ask a doctor if rash or irritation occurs.

WARNINGS SECTION


Warnings
For external use only
Do not use on broken skin

DOSAGE & ADMINISTRATION SECTION

Directions apply to underarms only

INACTIVE INGREDIENT SECTION

Inactive ingredients

Propylene glycol, fragrance, dibenzylidene sorbitol, diisopropyl sebacate, hydroxypropyl cellulose, PEG/PPG-14/4 dimethicone, tetrasodium EDTA.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Maximum Security

Antiperspirant

Regular

Net WT. 2.5 oz (70g)

image descriptionimage description

image of Backimage of Back

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
22431-641-012020-01-31C16284748780-19d75b9d0-407b-f424-e053-dadaa90a57ceMaximum Security Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
22431-641-01AntiperspirantMaximum Security70 g in 1 TUBESTICK702

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
22431-641ANTIPERSPIRANT MAXIMUM SECURITY (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX) STICK [BLUE CROSS LABS]2Legacy NDC, 1 package rows20181221_0d6fe25f-55dc-4bff-87f0-3f0578390c24.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
22431-64122431-641-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
DIISOPROPYL SEBACATEJ8T3X564IHIACT
HYDROXYPROPYL CELLULOSERFW2ET671PIACT

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
b5d7ca6f-3097-4e10-bb8a-f4b7b34af1690d6fe25f-55dc-4bff-87f0-3f0578390c242018-12-20WarningsExact identifier
spl id: b5d7ca6f-3097-4e10-bb8a-f4b7b34af169
spl set id: 0d6fe25f-55dc-4bff-87f0-3f0578390c24

Reported adverse events (FAERS/openFDA)#

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