Home NDC 73306-1191 ANTITRANSPIRANTE ABOVE MAXX EXTREME INVISIBLE
Product NDC 73306-1191
11-digit product format 733061191
Labeler code 73306
Product ID 73306-1191_4f467093-d681-2684-e063-6294a90a6ecf
Type HUMAN OTC DRUG
Nonproprietary name ANTITRANSPIRANTE ABOVE MAXX EXTREME INVISIBLE
Dosage form AEROSOL, SPRAY
Route TOPICAL
Labeler BASTON INDUSTRIA DE AEROSSOIS LTDA
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-04-12
Substance ALUMINUM SESQUICHLOROHYDRATE
Active strength 19.2 mg/150g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base ANTITRANSPIRANTE ABOVE MAXX EXTREME INVISIBLE
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM SESQUICHLOROHYDRATE 19.2 mg/150g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination UCN889409V Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73306-1191-1 ANTITRANSPIRANTE ABOVE MAXX EXTREME INVISIBLE 150 g in 1 BOTTLE, SPRAY AEROSOL, SPRAY 150 1
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 70 of 73 · 1,450 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 73306-1191-1 73306119101 150 g in 1 BOTTLE, SPRAY (73306-1191-1) 150 g 2026-04-12 No No Current