Antiperspirant Above Sport Energy Men

Manufacturer
Baston Industria de Aerossóis Ltda
Effective date
2024-10-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:24:04

Label at a glance#

ProductAntiperspirant Above Sport Energy Men
Active ingredientALUMINUM SESQUICHLOROHYDRATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABELPACKAGE LABEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73306-1113-1Antiperspirant Above Sport Energy Men90 g in 1 CANAEROSOL, SPRAY903

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73306-1113ANTIPERSPIRANT ABOVE SPORT ENERGY MEN (ANTIPERSPIRANT ABOVE SPORT ENERGY MEN AEROSOL) AEROSOL, SPRAY [BASTON INDUSTRIA DE AEROSSÓIS LTDA]3Current NDC, Legacy NDC, 1 package rows20241011_92ac5d7b-9ded-55ca-e053-2a95a90a3ff8.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
73306-111373306-1113-1

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

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 Sport Energy MenANTIPERSPIRANT ABOVE SPORT ENERGY MEN AEROSOLBaston Industria de Aerossis Ltda92ac5d7b-9ded-55ca-e053-2a95a90a3ff82024-10-09WarningsExact identifier
ndc (package): 73306-1113-1
ndc (product): 73306-1113
ndc11 (package): 73306111301
spl id: 240d2fac-2363-9351-e063-6394a90ae64d
spl set id: 92ac5d7b-9ded-55ca-e053-2a95a90a3ff8

Reported adverse events (FAERS/openFDA)#

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