Antiperspirant Above Country

Manufacturer
Baston Industria de Aerossóis Ltda
Effective date
2024-12-26
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:49:10

Label at a glance#

ProductAntiperspirant Above Country
Active ingredientALUMINUM SESQUICHLOROHYDRATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABEL PRINCIPAL COUNTRYPACKAGE LABEL PRINCIPAL COUNTRY

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73306-1102-1Antiperspirant Above Country90 g in 1 CANAEROSOL, SPRAY905

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73306-1102ANTIPERSPIRANT ABOVE COUNTRY (ANTIPERSPIRANT ABOVE COUNTRY AEROSOL) AEROSOL, SPRAY [BASTON INDUSTRIA DE AEROSSÓIS LTDA]5Current NDC, Legacy NDC, 1 package rows20241228_9231bd4f-53ba-04bb-e053-2a95a90a774b.zip

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73306-110273306-1102-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 matching rows.

Source Document#

Source XML · Source PDF

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
Antiperspirant Above CountryANTIPERSPIRANT ABOVE COUNTRY AEROSOLBaston Industria de Aerossis Ltda9231bd4f-53ba-04bb-e053-2a95a90a774b2024-12-26WarningsExact identifier
ndc (package): 73306-1102-1
ndc (product): 73306-1102
ndc11 (package): 73306110201
spl id: 2a2fbe3f-ef55-f4bd-e063-6294a90acbd0
spl set id: 9231bd4f-53ba-04bb-e053-2a95a90a774b

Reported adverse events (FAERS/openFDA)#

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