Home NDC 10596-337 Ban
Product NDC 10596-337
11-digit product format 105960337
Labeler code 10596
Product ID 10596-337_23fbdedd-afae-e476-e063-6294a90ac410
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Chlorohydrate
Dosage form LIQUID
Route TOPICAL
Labeler Kao USA Inc.
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-01-01
Substance ALUMINUM CHLOROHYDRATE
Active strength 20 g/103mL
NDC exclude flag No
Listing certified through 2026-12-31
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 Ban
Brand name suffix Roll-On Antiperspirant Deodorant Powder Fresh
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM CHLOROHYDRATE 20 g/103mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination HPN8MZW13M 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 10596-337-14 BanRoll-On Antiperspirant Deodorant Powder Fresh 103 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 103 10 10596-337-14 BanRoll-On Antiperspirant Deodorant Powder Fresh 4 in 1 PACKAGE LIQUID 4 10 10596-337-15 BanRoll-On Antiperspirant Deodorant Powder Fresh 44 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 44 10 10596-337-35 BanRoll-On Antiperspirant Deodorant Powder Fresh 103 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 103 10 10596-337-70 BanRoll-On Antiperspirant Deodorant Powder Fresh 103 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 103 10 10596-337-70 BanRoll-On Antiperspirant Deodorant Powder Fresh 2 in 1 PACKAGE LIQUID 2 10
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10596-337 BAN ROLL-ON ANTIPERSPIRANT DEODORANT POWDER FRESH (ALUMINUM CHLOROHYDRATE) LIQUID [KAO USA INC.] 10 Current NDC, Legacy NDC, 6 package rows 20241019_b99e8972-24e6-4f01-80f5-d071bbab8d30.zip
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 Marketing end Sample Exclude flag Status 10596-337-14 10596033714 4 BOTTLE, WITH APPLICATOR in 1 PACKAGE (10596-337-14) / 103 mL in 1 BOTTLE, WITH APPLICATOR 2020-08-24 0000-00-00 No No Current 10596-337-15 10596033715 44 mL in 1 BOTTLE, WITH APPLICATOR (10596-337-15) 44 ml 2016-10-08 0000-00-00 No No Current 10596-337-35 10596033735 103 mL in 1 BOTTLE, WITH APPLICATOR (10596-337-35) 103 ml 2012-01-01 0000-00-00 No No Current 10596-337-70 10596033770 2 BOTTLE, WITH APPLICATOR in 1 PACKAGE (10596-337-70) / 103 mL in 1 BOTTLE, WITH APPLICATOR 2016-09-12 0000-00-00 No No Current