Home NDC 73306-1183 ANTITRANSPIRANTE ABOVE ROLLON EXTREME BLACK
Product NDC 73306-1183
11-digit product format 733061183
Labeler code 73306
Product ID 73306-1183_4b263806-7dfe-7a3d-e063-6394a90a02b5
Type HUMAN OTC DRUG
Nonproprietary name ABOVE ROLLON EXTREME BLACK
Dosage form CREAM
Route TOPICAL
Labeler BASTON INDUSTRIA DE AEROSSOIS LTDA
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-02-19
Substance ALUMINUM CHLOROHYDRATE ANHYDROUS
Active strength 12 mg/50mL
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 ROLLON EXTREME BLACK
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM CHLOROHYDRATE ANHYDROUS 12 mg/50mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 407PSC3OC7 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 73306-1183-1 ANTITRANSPIRANTE ABOVE ROLLON EXTREME BLACK 50 mL in 1 BOTTLE, PLASTIC CREAM 50 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 73306-1183-1 73306118301 50 mL in 1 BOTTLE, PLASTIC (73306-1183-1) 50 ml 2026-02-19 No No Current