Home NDC 73306-1190 ANTITRANSPIRANTE ABOVE MAXX ORIGINAL
Product NDC 73306-1190
11-digit product format 733061190
Labeler code 73306
Product ID 73306-1190_4f45572f-f91f-063a-e063-6294a90a0113
Type HUMAN OTC DRUG
Nonproprietary name ANTITRANSPIRANTE ABOVE MAXX ORIGINAL
Dosage form CREAM
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/250mL
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 ORIGINAL
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM SESQUICHLOROHYDRATE 19.2 mg/250mL
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 73306-1190-1 ANTITRANSPIRANTE ABOVE MAXX ORIGINAL 250 mL in 1 BOTTLE, SPRAY CREAM 250 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 73306-1190-1 73306119001 250 mL in 1 BOTTLE, SPRAY (73306-1190-1) 250 ml 2026-04-12 No No Current