ABOVE EXTREME MEN MOVEMENT 72H SPRAY

Manufacturer
BASTON INDUSTRIA DE AEROSSOIS LTDA
Effective date
2024-07-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:15:05

Label at a glance#

ProductABOVE EXTREME MEN MOVEMENT 72 HOURS
Active ingredientALUMINUM SESQUICHLOROHYDRATE
Label structure2 sections

Label contents#

Full prescribing information#

OTC - QUESTIONS SECTION

EMAIL : SUPPORT@MYSPRAY.GROUP OR CALL (305) 677-5030

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABELLABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73306-1156-1ABOVE EXTREME MEN MOVEMENT 72 HOURS90 g in 1 BOTTLE, SPRAYAEROSOL, SPRAY902

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73306-1156ABOVE EXTREME MEN MOVEMENT 72 HOURS AEROSOL, SPRAY [BASTON INDUSTRIA DE AEROSSOIS LTDA]2Current NDC, 1 package rows20240711_fe8f7ad4-2a5a-ae30-e053-6394a90acb98.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73306-115673306-1156-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM SESQUICHLOROHYDRATEUCN889409VACTIB
ISOBUTANEBXR49TP611IACT

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
ABOVE EXTREME MEN MOVEMENT 72 HOURSABOVE EXTREME MEN MOVEMENT 72 HOURSBASTON INDUSTRIA DE AEROSSOIS LTDAfe8f7ad4-2a5a-ae30-e053-6394a90acb982024-07-09WarningsExact identifier
ndc (package): 73306-1156-1
ndc (product): 73306-1156
ndc11 (package): 73306115601
spl id: 1cd50ff1-3645-2add-e063-6394a90a482d
spl set id: fe8f7ad4-2a5a-ae30-e053-6394a90acb98

Reported adverse events (FAERS/openFDA)#

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